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Beschreibung
Retaining his excellent, proven approach, world-famous chemist and passionate teacher K.C. Nicolaou and his student Jason S. Chen compile here the important strategies and tools employed to construct complex molecules. Through 42 syntheses of 25 challenging natural products they explain the key steps of the synthetic pathway, highlighting the major developments for easier understanding, and contrasting these to other synthetic methods. Similar to its predecessors and completing a trilogy, this textbooks analyzes the syntheses in a didactic manner, with several chapters including mini-reviews of key methodologies, and an emphasis on the history, mechanism, scope, and generality of the reactions. In contrast to the first two volumes, this new one features full-color frontispieces.
A wonderful tool for learning and teaching, and a must-have for all current and future organic, medicinal and biological chemists.
From reviews of "Classics in Total Synthesis", Volumes I and II:
"...a volume, (...) which any chemist with an interest in synthetic organic chemistry will wish to acquire."
JACS
"...this superb book (...) will be an essential purchase for many organic chemists."
Nature
"... Classics II is undoubtedly an excellent bargain that is highly recommended to everybody interested in advanced organic chemistry..."
Angewandte Chemie
A wonderful tool for learning and teaching, and a must-have for all current and future organic, medicinal and biological chemists.
From reviews of "Classics in Total Synthesis", Volumes I and II:
"...a volume, (...) which any chemist with an interest in synthetic organic chemistry will wish to acquire."
JACS
"...this superb book (...) will be an essential purchase for many organic chemists."
Nature
"... Classics II is undoubtedly an excellent bargain that is highly recommended to everybody interested in advanced organic chemistry..."
Angewandte Chemie
Retaining his excellent, proven approach, world-famous chemist and passionate teacher K.C. Nicolaou and his student Jason S. Chen compile here the important strategies and tools employed to construct complex molecules. Through 42 syntheses of 25 challenging natural products they explain the key steps of the synthetic pathway, highlighting the major developments for easier understanding, and contrasting these to other synthetic methods. Similar to its predecessors and completing a trilogy, this textbooks analyzes the syntheses in a didactic manner, with several chapters including mini-reviews of key methodologies, and an emphasis on the history, mechanism, scope, and generality of the reactions. In contrast to the first two volumes, this new one features full-color frontispieces.
A wonderful tool for learning and teaching, and a must-have for all current and future organic, medicinal and biological chemists.
From reviews of "Classics in Total Synthesis", Volumes I and II:
"...a volume, (...) which any chemist with an interest in synthetic organic chemistry will wish to acquire."
JACS
"...this superb book (...) will be an essential purchase for many organic chemists."
Nature
"... Classics II is undoubtedly an excellent bargain that is highly recommended to everybody interested in advanced organic chemistry..."
Angewandte Chemie
A wonderful tool for learning and teaching, and a must-have for all current and future organic, medicinal and biological chemists.
From reviews of "Classics in Total Synthesis", Volumes I and II:
"...a volume, (...) which any chemist with an interest in synthetic organic chemistry will wish to acquire."
JACS
"...this superb book (...) will be an essential purchase for many organic chemists."
Nature
"... Classics II is undoubtedly an excellent bargain that is highly recommended to everybody interested in advanced organic chemistry..."
Angewandte Chemie
Über den Autor
K.C. Nicolaou holds joint appointments at The Scripps Research Institute, where he is the Chairman of the Department of Chemistry and holds the Darlene Shiley Chair in Chemistry and the Aline W. and L.S. Skaggs Professorship of Chemical Biology, and the University of California, San Diego, where he is Distinguished Professor of Chemistry. His impact on chemistry, biology and medicine flows from his research works in chemical synthesis and chemical biology described in numerous publications and patens. For his contributions to science and education, he was elected Fellow of the New York Academy of Sciences, Fellow of the American Academy of Arts and Sciences, Member of the National Academy of Sciences, USA, Member of the German Academy of Sciences Leopoldina, and Corresponding Member of the Academy of Athens, Greece. He is the recipient of many prizes, awards and honors.
Jason S. Chen received his A.B. and A.M. degrees in Chemistry from Harvard University in 2001. After two years as a medicinal chemist at Enanta Pharmaceuticals, he began graduate studies at The Scripps Research Institute under the guidance of Professor K.C. Nicolaou. He received a National Defense Science and Engineering Graduate fellowship, and completed his Ph.D. studies in 2008. He currently is a post-doctoral fellow in Professor Nicolaou's laboratory.
Jason S. Chen received his A.B. and A.M. degrees in Chemistry from Harvard University in 2001. After two years as a medicinal chemist at Enanta Pharmaceuticals, he began graduate studies at The Scripps Research Institute under the guidance of Professor K.C. Nicolaou. He received a National Defense Science and Engineering Graduate fellowship, and completed his Ph.D. studies in 2008. He currently is a post-doctoral fellow in Professor Nicolaou's laboratory.
Inhaltsverzeichnis
INTRODUCTION: THE ADVANCING FIELD OF TOTAL SYNTHESIS
Targets
Strategies and Methods
Classics in Total Synthesis III
TETRODOTOXIN
Introduction
Kishi's Retrosynthetic Analysis and Strategy
Kishi's Total Synthesis
Du Bois' Retrosynthetic Analysis and Strategy
Du Bois' Total Synthesis
Conclusion
DISCODERMOLIDE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
AZASPIRACID-1
Introduction
Nicolaou's Retrosynthetic Analysis and Strategy
Nicolaou's Total Synthesis
Evans' Retrosynthetic Analysis and Strategy
Evans' Total Synthesis
Conclusion
THIOSTREPTON
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
PENTACYCLOANAMMOXIC ACID METHYL ESTER
Introduction
First-Generation Retrosynthetic Analysis and Strategy
First-Generation Total Synthesis
Second-Generation Retrosynthetic Analysis and Strategy
Second-Generation Total Synthesis
Conclusion
LITTORALISONE, OSELTAMIVIR (TAMIFLU®), AND HIRSUTELLONE B
Introduction
Introduction to Littoralisone
Total Synthesis of Littoralisone
Introduction to Oseltamivir (Tamiflu®)
Total Synthesis of Oseltamivir (Tamiflu®)
Introduction to Hirsutellone B
Total Synthesis of Hirsutellone B
Conclusion
RUBICORDIFOLIN AND RUBIONCOLIN B
Introduction
Retrosynthetic Analysis of Rubicordifolin
Total Synthesis of Rubicordifolin
Retrosyntheticd Analysis of Rubioncolin B
Total Synthesis of Rubioncolin B
Conclusion
CYANTHIWIGINS U AND F
Introduction
Phillips' Retrosynthetic Analysis and Strategy
Phillips' Total Synthesis
Stolz' Retrosynthetic Analysis and Strategy
Stoltz' Total Synthesis
Conclusion
STEPHACIDIN B
Introduction
Myers' Retrosynthetic Analysis and Strategy
Meyers' Total Synthesis
Baran's Retrosynthetic Analysis and Strategy
Baran's Total Synthesis
Williams' Retrosynthetic Analysis and Strategy
Williams' Total Synthesis
Conclusion
ABYSSOMICIN C AND ATROP-ABYSSOMICIN C
Introduction
Sorensen's Retrosynthetic Analysis and Strategy
Sorensen's Total Synthesis of Abyssomicin C
Nicolaou's Retrosynthetic Analysis and Strategy
Nicolaou's Total Synthesis of Abyssomicin C and atrop-Abyssomicin C
Conclusion
TETRACYCLINE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
BISANTHRAQUINONE NATURAL PRODUCTS
Introduction
Retrosynthetic Analysis and Strategy Toward 2,2'-epi-Cytoskyrin A, Rugulosin, and Rugulin
Total Synthesis of 2,2'-epi-Cytoskyrin A, Rugulosin, and Rugulin
Retrosynthetic Analysis and Strategy Toward Antibiotic BE-43472B
Total Synthesis of Antibiotic BE-43472B
Conclusion
GARSUBELLIN A
Introduction
Sibasaki and Kanai's Retrosynthetic Analysis and Strategy
Shibasaki and Kanai's Total Synthesis
Danishefsky's Retrosynthetic Analysis and Strategy
Danishefsky's Total Synthesis
Conclusion
WELWITINDOLINONE A
Introduction
Baran's Retrosynthetic Analysis and Strategy
Barans' Total Synthesis
Wood's Retrosynthetic Analysis and Strategy
Wood's Total Synthesis
Conclusion
IEJIMALIDE B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
KEDARCIDIN CHROMOPHORE AND MADUROPEPTIN CHROMOPHORE
Introduction
Retrosynthetic Analysis and Strategy for Kedarcidin Chromophore
Total Synthesis of Kedarcidin Chromophore
Retrosynthetic Analysis and Strategy for Maduropeptin Chromophore
Total Synthesis of Maduropeptin Chromophore
Conclusion
BIYOUYANAGIN A
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
AZADIRACHTIN
Introduction
Retrosynthetic Analysis and Strategy
Synthesis
Conclusion
RESVERATROL-DERIVED NATURAL PRODUCTS
Introduction
Snyder's Retrosynthetic Analysis and Strategy for a Collection of Resveratrol-Derived Natural Products
Snyder's Total Synthesis of a Collection of Resveratrol-Derived Natural Products
Nicolaou and Chen's Retrosynthetic Analysis and Strategy for Hopeahainol A and Hopeanol
Nicolaou and Chen's Total Synthesis of Hopeahainol A and Hopeanol
Conclusion
CHLOROSULFOLIPID CYTOTOXIN
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
SPOROLIDE B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
11,11'-DIDEOXYVERTICILLIN A AND CHAETOCIN
Introduction
Retrosynthetic Analysis and Strategy for 11,11'-Dideoxyverticillin A
Total Synthesis of 11,11'-Dideoxyverticillin A
Retrosynthetic Analysis and Strategy for Chaetocin
Total Synthesis of Chaetocin
Conclusion
VANNUSAL B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
HAPLOPHYTINE
Introduction
Fukuyama and Tokuyama's Retrosynthetic Analysis and Strategy
Fukuyama and Tokuyama's Total Synthesis
Nicolaou and Chen's Retrosynthetic Analysis and Strategy
Nicolaou and Chen's Total Synthesis
Conclusion
PALAU'AMINE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
Targets
Strategies and Methods
Classics in Total Synthesis III
TETRODOTOXIN
Introduction
Kishi's Retrosynthetic Analysis and Strategy
Kishi's Total Synthesis
Du Bois' Retrosynthetic Analysis and Strategy
Du Bois' Total Synthesis
Conclusion
DISCODERMOLIDE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
AZASPIRACID-1
Introduction
Nicolaou's Retrosynthetic Analysis and Strategy
Nicolaou's Total Synthesis
Evans' Retrosynthetic Analysis and Strategy
Evans' Total Synthesis
Conclusion
THIOSTREPTON
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
PENTACYCLOANAMMOXIC ACID METHYL ESTER
Introduction
First-Generation Retrosynthetic Analysis and Strategy
First-Generation Total Synthesis
Second-Generation Retrosynthetic Analysis and Strategy
Second-Generation Total Synthesis
Conclusion
LITTORALISONE, OSELTAMIVIR (TAMIFLU®), AND HIRSUTELLONE B
Introduction
Introduction to Littoralisone
Total Synthesis of Littoralisone
Introduction to Oseltamivir (Tamiflu®)
Total Synthesis of Oseltamivir (Tamiflu®)
Introduction to Hirsutellone B
Total Synthesis of Hirsutellone B
Conclusion
RUBICORDIFOLIN AND RUBIONCOLIN B
Introduction
Retrosynthetic Analysis of Rubicordifolin
Total Synthesis of Rubicordifolin
Retrosyntheticd Analysis of Rubioncolin B
Total Synthesis of Rubioncolin B
Conclusion
CYANTHIWIGINS U AND F
Introduction
Phillips' Retrosynthetic Analysis and Strategy
Phillips' Total Synthesis
Stolz' Retrosynthetic Analysis and Strategy
Stoltz' Total Synthesis
Conclusion
STEPHACIDIN B
Introduction
Myers' Retrosynthetic Analysis and Strategy
Meyers' Total Synthesis
Baran's Retrosynthetic Analysis and Strategy
Baran's Total Synthesis
Williams' Retrosynthetic Analysis and Strategy
Williams' Total Synthesis
Conclusion
ABYSSOMICIN C AND ATROP-ABYSSOMICIN C
Introduction
Sorensen's Retrosynthetic Analysis and Strategy
Sorensen's Total Synthesis of Abyssomicin C
Nicolaou's Retrosynthetic Analysis and Strategy
Nicolaou's Total Synthesis of Abyssomicin C and atrop-Abyssomicin C
Conclusion
TETRACYCLINE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
BISANTHRAQUINONE NATURAL PRODUCTS
Introduction
Retrosynthetic Analysis and Strategy Toward 2,2'-epi-Cytoskyrin A, Rugulosin, and Rugulin
Total Synthesis of 2,2'-epi-Cytoskyrin A, Rugulosin, and Rugulin
Retrosynthetic Analysis and Strategy Toward Antibiotic BE-43472B
Total Synthesis of Antibiotic BE-43472B
Conclusion
GARSUBELLIN A
Introduction
Sibasaki and Kanai's Retrosynthetic Analysis and Strategy
Shibasaki and Kanai's Total Synthesis
Danishefsky's Retrosynthetic Analysis and Strategy
Danishefsky's Total Synthesis
Conclusion
WELWITINDOLINONE A
Introduction
Baran's Retrosynthetic Analysis and Strategy
Barans' Total Synthesis
Wood's Retrosynthetic Analysis and Strategy
Wood's Total Synthesis
Conclusion
IEJIMALIDE B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
KEDARCIDIN CHROMOPHORE AND MADUROPEPTIN CHROMOPHORE
Introduction
Retrosynthetic Analysis and Strategy for Kedarcidin Chromophore
Total Synthesis of Kedarcidin Chromophore
Retrosynthetic Analysis and Strategy for Maduropeptin Chromophore
Total Synthesis of Maduropeptin Chromophore
Conclusion
BIYOUYANAGIN A
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
AZADIRACHTIN
Introduction
Retrosynthetic Analysis and Strategy
Synthesis
Conclusion
RESVERATROL-DERIVED NATURAL PRODUCTS
Introduction
Snyder's Retrosynthetic Analysis and Strategy for a Collection of Resveratrol-Derived Natural Products
Snyder's Total Synthesis of a Collection of Resveratrol-Derived Natural Products
Nicolaou and Chen's Retrosynthetic Analysis and Strategy for Hopeahainol A and Hopeanol
Nicolaou and Chen's Total Synthesis of Hopeahainol A and Hopeanol
Conclusion
CHLOROSULFOLIPID CYTOTOXIN
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
SPOROLIDE B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
11,11'-DIDEOXYVERTICILLIN A AND CHAETOCIN
Introduction
Retrosynthetic Analysis and Strategy for 11,11'-Dideoxyverticillin A
Total Synthesis of 11,11'-Dideoxyverticillin A
Retrosynthetic Analysis and Strategy for Chaetocin
Total Synthesis of Chaetocin
Conclusion
VANNUSAL B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
HAPLOPHYTINE
Introduction
Fukuyama and Tokuyama's Retrosynthetic Analysis and Strategy
Fukuyama and Tokuyama's Total Synthesis
Nicolaou and Chen's Retrosynthetic Analysis and Strategy
Nicolaou and Chen's Total Synthesis
Conclusion
PALAU'AMINE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
Details
Erscheinungsjahr: | 2011 |
---|---|
Fachbereich: | Organische Chemie |
Genre: | Chemie |
Rubrik: | Naturwissenschaften & Technik |
Medium: | Taschenbuch |
Inhalt: |
XXIV
746 S. 26 farbige Illustr. 26 Illustr. |
ISBN-13: | 9783527329571 |
ISBN-10: | 3527329579 |
Sprache: | Englisch |
Herstellernummer: | 1132957 000 |
Einband: | Kartoniert / Broschiert |
Autor: |
Nicolaou, K. C.
Chen, Jason S. |
Hersteller: | Wiley-VCH GmbH |
Maße: | 256 x 194 x 33 mm |
Von/Mit: | K. C. Nicolaou (u. a.) |
Erscheinungsdatum: | 09.02.2011 |
Gewicht: | 1,667 kg |
Über den Autor
K.C. Nicolaou holds joint appointments at The Scripps Research Institute, where he is the Chairman of the Department of Chemistry and holds the Darlene Shiley Chair in Chemistry and the Aline W. and L.S. Skaggs Professorship of Chemical Biology, and the University of California, San Diego, where he is Distinguished Professor of Chemistry. His impact on chemistry, biology and medicine flows from his research works in chemical synthesis and chemical biology described in numerous publications and patens. For his contributions to science and education, he was elected Fellow of the New York Academy of Sciences, Fellow of the American Academy of Arts and Sciences, Member of the National Academy of Sciences, USA, Member of the German Academy of Sciences Leopoldina, and Corresponding Member of the Academy of Athens, Greece. He is the recipient of many prizes, awards and honors.
Jason S. Chen received his A.B. and A.M. degrees in Chemistry from Harvard University in 2001. After two years as a medicinal chemist at Enanta Pharmaceuticals, he began graduate studies at The Scripps Research Institute under the guidance of Professor K.C. Nicolaou. He received a National Defense Science and Engineering Graduate fellowship, and completed his Ph.D. studies in 2008. He currently is a post-doctoral fellow in Professor Nicolaou's laboratory.
Jason S. Chen received his A.B. and A.M. degrees in Chemistry from Harvard University in 2001. After two years as a medicinal chemist at Enanta Pharmaceuticals, he began graduate studies at The Scripps Research Institute under the guidance of Professor K.C. Nicolaou. He received a National Defense Science and Engineering Graduate fellowship, and completed his Ph.D. studies in 2008. He currently is a post-doctoral fellow in Professor Nicolaou's laboratory.
Inhaltsverzeichnis
INTRODUCTION: THE ADVANCING FIELD OF TOTAL SYNTHESIS
Targets
Strategies and Methods
Classics in Total Synthesis III
TETRODOTOXIN
Introduction
Kishi's Retrosynthetic Analysis and Strategy
Kishi's Total Synthesis
Du Bois' Retrosynthetic Analysis and Strategy
Du Bois' Total Synthesis
Conclusion
DISCODERMOLIDE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
AZASPIRACID-1
Introduction
Nicolaou's Retrosynthetic Analysis and Strategy
Nicolaou's Total Synthesis
Evans' Retrosynthetic Analysis and Strategy
Evans' Total Synthesis
Conclusion
THIOSTREPTON
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
PENTACYCLOANAMMOXIC ACID METHYL ESTER
Introduction
First-Generation Retrosynthetic Analysis and Strategy
First-Generation Total Synthesis
Second-Generation Retrosynthetic Analysis and Strategy
Second-Generation Total Synthesis
Conclusion
LITTORALISONE, OSELTAMIVIR (TAMIFLU®), AND HIRSUTELLONE B
Introduction
Introduction to Littoralisone
Total Synthesis of Littoralisone
Introduction to Oseltamivir (Tamiflu®)
Total Synthesis of Oseltamivir (Tamiflu®)
Introduction to Hirsutellone B
Total Synthesis of Hirsutellone B
Conclusion
RUBICORDIFOLIN AND RUBIONCOLIN B
Introduction
Retrosynthetic Analysis of Rubicordifolin
Total Synthesis of Rubicordifolin
Retrosyntheticd Analysis of Rubioncolin B
Total Synthesis of Rubioncolin B
Conclusion
CYANTHIWIGINS U AND F
Introduction
Phillips' Retrosynthetic Analysis and Strategy
Phillips' Total Synthesis
Stolz' Retrosynthetic Analysis and Strategy
Stoltz' Total Synthesis
Conclusion
STEPHACIDIN B
Introduction
Myers' Retrosynthetic Analysis and Strategy
Meyers' Total Synthesis
Baran's Retrosynthetic Analysis and Strategy
Baran's Total Synthesis
Williams' Retrosynthetic Analysis and Strategy
Williams' Total Synthesis
Conclusion
ABYSSOMICIN C AND ATROP-ABYSSOMICIN C
Introduction
Sorensen's Retrosynthetic Analysis and Strategy
Sorensen's Total Synthesis of Abyssomicin C
Nicolaou's Retrosynthetic Analysis and Strategy
Nicolaou's Total Synthesis of Abyssomicin C and atrop-Abyssomicin C
Conclusion
TETRACYCLINE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
BISANTHRAQUINONE NATURAL PRODUCTS
Introduction
Retrosynthetic Analysis and Strategy Toward 2,2'-epi-Cytoskyrin A, Rugulosin, and Rugulin
Total Synthesis of 2,2'-epi-Cytoskyrin A, Rugulosin, and Rugulin
Retrosynthetic Analysis and Strategy Toward Antibiotic BE-43472B
Total Synthesis of Antibiotic BE-43472B
Conclusion
GARSUBELLIN A
Introduction
Sibasaki and Kanai's Retrosynthetic Analysis and Strategy
Shibasaki and Kanai's Total Synthesis
Danishefsky's Retrosynthetic Analysis and Strategy
Danishefsky's Total Synthesis
Conclusion
WELWITINDOLINONE A
Introduction
Baran's Retrosynthetic Analysis and Strategy
Barans' Total Synthesis
Wood's Retrosynthetic Analysis and Strategy
Wood's Total Synthesis
Conclusion
IEJIMALIDE B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
KEDARCIDIN CHROMOPHORE AND MADUROPEPTIN CHROMOPHORE
Introduction
Retrosynthetic Analysis and Strategy for Kedarcidin Chromophore
Total Synthesis of Kedarcidin Chromophore
Retrosynthetic Analysis and Strategy for Maduropeptin Chromophore
Total Synthesis of Maduropeptin Chromophore
Conclusion
BIYOUYANAGIN A
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
AZADIRACHTIN
Introduction
Retrosynthetic Analysis and Strategy
Synthesis
Conclusion
RESVERATROL-DERIVED NATURAL PRODUCTS
Introduction
Snyder's Retrosynthetic Analysis and Strategy for a Collection of Resveratrol-Derived Natural Products
Snyder's Total Synthesis of a Collection of Resveratrol-Derived Natural Products
Nicolaou and Chen's Retrosynthetic Analysis and Strategy for Hopeahainol A and Hopeanol
Nicolaou and Chen's Total Synthesis of Hopeahainol A and Hopeanol
Conclusion
CHLOROSULFOLIPID CYTOTOXIN
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
SPOROLIDE B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
11,11'-DIDEOXYVERTICILLIN A AND CHAETOCIN
Introduction
Retrosynthetic Analysis and Strategy for 11,11'-Dideoxyverticillin A
Total Synthesis of 11,11'-Dideoxyverticillin A
Retrosynthetic Analysis and Strategy for Chaetocin
Total Synthesis of Chaetocin
Conclusion
VANNUSAL B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
HAPLOPHYTINE
Introduction
Fukuyama and Tokuyama's Retrosynthetic Analysis and Strategy
Fukuyama and Tokuyama's Total Synthesis
Nicolaou and Chen's Retrosynthetic Analysis and Strategy
Nicolaou and Chen's Total Synthesis
Conclusion
PALAU'AMINE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
Targets
Strategies and Methods
Classics in Total Synthesis III
TETRODOTOXIN
Introduction
Kishi's Retrosynthetic Analysis and Strategy
Kishi's Total Synthesis
Du Bois' Retrosynthetic Analysis and Strategy
Du Bois' Total Synthesis
Conclusion
DISCODERMOLIDE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
AZASPIRACID-1
Introduction
Nicolaou's Retrosynthetic Analysis and Strategy
Nicolaou's Total Synthesis
Evans' Retrosynthetic Analysis and Strategy
Evans' Total Synthesis
Conclusion
THIOSTREPTON
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
PENTACYCLOANAMMOXIC ACID METHYL ESTER
Introduction
First-Generation Retrosynthetic Analysis and Strategy
First-Generation Total Synthesis
Second-Generation Retrosynthetic Analysis and Strategy
Second-Generation Total Synthesis
Conclusion
LITTORALISONE, OSELTAMIVIR (TAMIFLU®), AND HIRSUTELLONE B
Introduction
Introduction to Littoralisone
Total Synthesis of Littoralisone
Introduction to Oseltamivir (Tamiflu®)
Total Synthesis of Oseltamivir (Tamiflu®)
Introduction to Hirsutellone B
Total Synthesis of Hirsutellone B
Conclusion
RUBICORDIFOLIN AND RUBIONCOLIN B
Introduction
Retrosynthetic Analysis of Rubicordifolin
Total Synthesis of Rubicordifolin
Retrosyntheticd Analysis of Rubioncolin B
Total Synthesis of Rubioncolin B
Conclusion
CYANTHIWIGINS U AND F
Introduction
Phillips' Retrosynthetic Analysis and Strategy
Phillips' Total Synthesis
Stolz' Retrosynthetic Analysis and Strategy
Stoltz' Total Synthesis
Conclusion
STEPHACIDIN B
Introduction
Myers' Retrosynthetic Analysis and Strategy
Meyers' Total Synthesis
Baran's Retrosynthetic Analysis and Strategy
Baran's Total Synthesis
Williams' Retrosynthetic Analysis and Strategy
Williams' Total Synthesis
Conclusion
ABYSSOMICIN C AND ATROP-ABYSSOMICIN C
Introduction
Sorensen's Retrosynthetic Analysis and Strategy
Sorensen's Total Synthesis of Abyssomicin C
Nicolaou's Retrosynthetic Analysis and Strategy
Nicolaou's Total Synthesis of Abyssomicin C and atrop-Abyssomicin C
Conclusion
TETRACYCLINE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
BISANTHRAQUINONE NATURAL PRODUCTS
Introduction
Retrosynthetic Analysis and Strategy Toward 2,2'-epi-Cytoskyrin A, Rugulosin, and Rugulin
Total Synthesis of 2,2'-epi-Cytoskyrin A, Rugulosin, and Rugulin
Retrosynthetic Analysis and Strategy Toward Antibiotic BE-43472B
Total Synthesis of Antibiotic BE-43472B
Conclusion
GARSUBELLIN A
Introduction
Sibasaki and Kanai's Retrosynthetic Analysis and Strategy
Shibasaki and Kanai's Total Synthesis
Danishefsky's Retrosynthetic Analysis and Strategy
Danishefsky's Total Synthesis
Conclusion
WELWITINDOLINONE A
Introduction
Baran's Retrosynthetic Analysis and Strategy
Barans' Total Synthesis
Wood's Retrosynthetic Analysis and Strategy
Wood's Total Synthesis
Conclusion
IEJIMALIDE B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
KEDARCIDIN CHROMOPHORE AND MADUROPEPTIN CHROMOPHORE
Introduction
Retrosynthetic Analysis and Strategy for Kedarcidin Chromophore
Total Synthesis of Kedarcidin Chromophore
Retrosynthetic Analysis and Strategy for Maduropeptin Chromophore
Total Synthesis of Maduropeptin Chromophore
Conclusion
BIYOUYANAGIN A
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
AZADIRACHTIN
Introduction
Retrosynthetic Analysis and Strategy
Synthesis
Conclusion
RESVERATROL-DERIVED NATURAL PRODUCTS
Introduction
Snyder's Retrosynthetic Analysis and Strategy for a Collection of Resveratrol-Derived Natural Products
Snyder's Total Synthesis of a Collection of Resveratrol-Derived Natural Products
Nicolaou and Chen's Retrosynthetic Analysis and Strategy for Hopeahainol A and Hopeanol
Nicolaou and Chen's Total Synthesis of Hopeahainol A and Hopeanol
Conclusion
CHLOROSULFOLIPID CYTOTOXIN
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
SPOROLIDE B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
11,11'-DIDEOXYVERTICILLIN A AND CHAETOCIN
Introduction
Retrosynthetic Analysis and Strategy for 11,11'-Dideoxyverticillin A
Total Synthesis of 11,11'-Dideoxyverticillin A
Retrosynthetic Analysis and Strategy for Chaetocin
Total Synthesis of Chaetocin
Conclusion
VANNUSAL B
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
HAPLOPHYTINE
Introduction
Fukuyama and Tokuyama's Retrosynthetic Analysis and Strategy
Fukuyama and Tokuyama's Total Synthesis
Nicolaou and Chen's Retrosynthetic Analysis and Strategy
Nicolaou and Chen's Total Synthesis
Conclusion
PALAU'AMINE
Introduction
Retrosynthetic Analysis and Strategy
Total Synthesis
Conclusion
Details
Erscheinungsjahr: | 2011 |
---|---|
Fachbereich: | Organische Chemie |
Genre: | Chemie |
Rubrik: | Naturwissenschaften & Technik |
Medium: | Taschenbuch |
Inhalt: |
XXIV
746 S. 26 farbige Illustr. 26 Illustr. |
ISBN-13: | 9783527329571 |
ISBN-10: | 3527329579 |
Sprache: | Englisch |
Herstellernummer: | 1132957 000 |
Einband: | Kartoniert / Broschiert |
Autor: |
Nicolaou, K. C.
Chen, Jason S. |
Hersteller: | Wiley-VCH GmbH |
Maße: | 256 x 194 x 33 mm |
Von/Mit: | K. C. Nicolaou (u. a.) |
Erscheinungsdatum: | 09.02.2011 |
Gewicht: | 1,667 kg |
Warnhinweis