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140627s1994 ne a o 000 0 eng d |
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|a OPELS
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|a 937405243
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|a 9781483163536
|q (electronic bk.)
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|a 1483163539
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|z 0444817808
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|z 9780444817808
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|a (OCoLC)881849528
|z (OCoLC)937405243
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|a QD415
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|a SCI
|x 013040
|2 bisacsh
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|a 547.7
|2 22
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|a Studies in natural products chemistry /
|c edited by Atta-ur-Rahman.
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|a Amsterdam ;
|a London :
|b Elsevier.
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|a 1 online resource (xiv, 924 pages)
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|a text
|b txt
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|a computer
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|a online resource
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|a Studies in Natural Products Chemistry ;
|v v. 14
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|a Print version record.
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|a Front Cover; Stereoselective Synthesis (Part I); Copyright Page; Table of Contents; FOREWORD; PREFACE; CONTRIBUTORS; Stereoselective Synthesis; CHAPTER 1. STEREOSELECTIVE SYNTHESES OF DOXORUBICIN AND RELATED COMPOUNDS; 1 INTRODUCTION; 2 SURVEY OF STEREOSELECTIVE SYNTHESES; 3 DERIVATIVES OF DOXORUBICIN; 4 A NEW SYNTHESIS OF DAUNOMYCINONE AND SOME ANALOGUES; ACKNOWLEDGEMENTS; REFERENCES; CHAPTER 2. TOTAL SYNTHESIS OF NOGALAMYCIN CONGENERS AND THEIR RELATED COMPOUNDS ; 1. Introduction; 2. Synthetic Strategy; 3. Chrial Synthesis of the DEF-Ring System of Nogalamycin.
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|a 4. Chrial Synthesis of the CDEF-Ring System of Nogalamycin5. Total Synthesis of (+)-Nogarene; 6. Total Synthesis of (+)-7-Deoxynogarol; 7. Total Synthesis of (+)-7-con-O-Methylnogarol; 8. Synthesis and Antitumor Activity of Various Nogalamycin Congeners; 9. Total Synthesis of (�)-7-con-O-Methylnogarol; 10. Conclusion; Acknowledgements; References and Notes; CHAPTER 3. SYNTHESIS OF THE TETRANIIC ACID ANTIBIOTICS; Introduction; Characterization; Biosynthesis; Biological Activity; Acknowledgments; References; CHAPTER 4. The Syntheses of 3- and 4-Deoxy-hexoses; 1. Introduction.
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|a 2. The 3'-Deoxy-aminoglycoside Antibiotics3. The 3-Deoxy and 4-Deoxyhexoses as Biochemical Tools; 4. The Selective Deoxygenation of Common Sugars; 5. The Homologation of 2-Deoxyrentoses; 6. Total Asymmetric Syntheses Applying Enzymatic Processes; 7. Total Syntheses Applying Diels-Alder Additions; 8. Other Synthetic Approaches to 3- and 4-Deoxyhexoses; 9. The Syntheses of D- and L-Lividosamine; REFERENCES; CHAPTER 5. RECENT DEVELOPMENTS IN THE SYNTHESIS OF POLYSACCHARIDES AND STEREOSPECSFICITY OF GLYCOSYLATION REACTIONS; 1. INTRODUCTION; 2. STEREOSPECIPICITY OF GLYCOSYLATION.
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|a 3. PROGRESS IN THE SYNTHESIS OF POLYSACCHARIDES WITH REGULAR STRUCTURE4. ON SYNTHESIS OF POLYSACCHARIDES BY OTHER METHODS; REFERENCES; CHAPTER 6. LEVOGLUCOSENONE: A VERSATILE CARBOHYDRATE PRECURSOR FOR THE SYNTHESIS OF NATURAL PRODUCTS; 1. INTRODUCTION; 2. PHYSICO-CHEMICAL PROPERTIES; 3. ISOLATION AND SYNTHESIS; 4. REACTION OF CARBONYL GROUP; 5. REACTION OF DOUBLE BOND; 6. CUCLOADDITION; 7. MICHAEL ADDITION REACTIONS; S. MISCELLANEOUS REACTIONS; 9. CONCLUSION; REFERENCES; CHAPTER 7. Chemical Synthesis of Branched Oligoribonucleotides and their Related Compounds; 1. INTRODUCTION.
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|a 2. THE SYNTHESIS OF BRANCHED RNA BY THE USE OF 2',3'-BISPHOSPHORYLATED RIBONUCLEOSIDE UNITS3. THE SYNTESIS OF BRANCHED RNA BY THE USE OF SYNTHETIC UNIT (16) HAVING 3'-BIS(2-CYANOETHOXY)PHOSPHORYI. GROUP; 4. OTHER METHODS FOR THE SYNTHESIS OF BRANCHED OLIGORIBONUCLEOTIDES; 5. SYNTHESIS OF 2'-PHOSPHORYLATED OLIGORIBONUCLEOTIDES; REFERENCES; CHAPTER 8. Oxidation Products of Guaiazulene and Other Azulenic Hydrocarbons; 1 INTRODUCTION; 2 OXIDATION OF GUAIAZULENE; 3 OXIDATION OF AZULENE; 4 OXIDATION OF MONO-SUBSTITUTED AZULENES; 5 OXIDATION OF DI-SUBSTITUTED AZULENES.
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|a Stereochemistry.
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|a Organic compounds
|x Synthesis.
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|a St�er�eochimie.
|0 (CaQQLa)201-0002577
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|a Compos�es organiques
|x Synth�ese.
|0 (CaQQLa)201-0020323
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|a SCIENCE
|x Chemistry
|x Organic.
|2 bisacsh
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|a Organic compounds
|x Synthesis.
|2 fast
|0 (OCoLC)fst01047668
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|a Stereochemistry.
|2 fast
|0 (OCoLC)fst01133138
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700 |
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|a Rahman, Atta-ur-,
|d 1942-
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776 |
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8 |
|i Print version:
|t Studies in natural products chemistry
|z 0444817808
|w (OCoLC)30033040
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830 |
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0 |
|a Studies in natural products chemistry.
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856 |
4 |
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|u https://sciencedirect.uam.elogim.com/science/book/9780444817808
|z Texto completo
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856 |
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|u https://sciencedirect.uam.elogim.com/science/bookseries/15725995/14/part/PI
|z Texto completo
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