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cr cnu---unuuu |
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141029s1970 enka ob 100 0 eng d |
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|a OPELS
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|a 895435160
|a 1162233578
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|a 9781483284675
|q (electronic bk.)
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|a 1483284670
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|z 9780408700948
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|a (OCoLC)893979576
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|a 572
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|a International Symposium on the Chemistry of Natural Products
|n (6th :
|d 1969 :
|c Mexico City, Mexico)
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|a The chemistry of natural products, 6 :
|b plenary lectures presented at the sixth International Symposium on the Chemistry of Natural Products, held in Mexico City, Mexico, 21-25 April 1969.
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|a London :
|b Butterworths,
|c [1970]
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300 |
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|a 1 online resource (pages 123-293.) :
|b illustrations
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
|2 rdamedia
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|a online resource
|b cr
|2 rdacarrier
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|a Sponsored by the International Union of Pure and Applied Chemistry, Organic Chemistry DIvision, in conjunction with Mexican Chemical Society.
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|a Contents appear in Pure and applied chemistry, v.2l, no. 2 1970.
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|a Includes bibliographical references.
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|a Print version record.
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|6 880-01
|a Front Cover; The Chemistry of Natural Products 6; Copyright Page; Table of Contents; CHAPTER 1. RECENT STUDIES ON SESQUITERPENES; ABSTRACT; INTRODUCTION; APPENDIX; References; CHAPTER 2. RECENT ADVANCES IN THE CHEMISTRY OF PLANT STEROIDS; ABSTRACT; INTRODUCTION; STEROIDAL SAPONINS; STEROIDAL ALKALOIDS; Acknowledgement; References; CHAPTER 3. ARDENOLIDES AND RELATED PRODUCTS; ABSTRACT; HISTORICAL; MODIFICATIONS OF THE CARDENOLIDE STRUCTURE; References; CHAPTER 4. CHEMICAL CONTRIBUTIONS TO TAXONOMY AND PHYLOGENY IN THE GENUS ARTEMISIA; ABSTRACT; INTRODUCTION.
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|a THE SESQUITERPENE LACTONE CONSTITUENTSRELATED GENERA OF THE TRIBE; SUMMARY; Acknowledgement; References; CHAPTER 5. SESQUITERPENES HAVING A FIVE-MEMBERED ETHER-RING IN THE MOLECULE; ABSTRACT; INTRODUCTION; I. OXIDATION OF GUAIOXIDE WITH MICRO-ORGANISMS; II. A NEW FURAN SESQUITERPENE HAVING A CYCLOPROPANE-RING (STRUCTURE OF LINDENENE); III. ON GERMACRANE-TYPE FURAN SESQUITERPENES; IV. SOME CHEMOTAXONOMICAL PROBLEMS; CONCLUSION; References; CHAPTER 6. APPLICATIONS OF MASS SPECTROMETRY IN THE STEROID FIELD; ABSTRACT; INTRODUCTION; DETERMINATION OF EMPIRICAL FORMULA.
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|a The Chemistry of Natural Products: 6 discusses some of the advances in the chemistry of sesquiterpenic lactones. This book presents the studies on terpenoids isolated from Compositae. Organized into 10 chapters, this book begins with an overview of the revised structures of some guaianolides and germacranolides. This text then examines the advances in the field of steroidal alkaloids and sapogenins possessing the C27-carbon skeleton of cholestane. Other chapters consider the usefulness of steroidal glycosides of digitalis as life-saving products. This book discusses as well the microbiological.
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|a English.
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650 |
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|a Biochemistry
|v Congresses.
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6 |
|a Biochimie
|0 (CaQQLa)201-0001077
|v Congr�es.
|0 (CaQQLa)201-0378219
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650 |
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|a SCIENCE
|x Life Sciences
|x Biochemistry.
|2 bisacsh
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|a Biochemistry
|2 fast
|0 (OCoLC)fst00831961
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|a Congress
|0 (DNLM)D016423
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|a proceedings (reports)
|2 aat
|0 (CStmoGRI)aatgf300027316
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|a Conference papers and proceedings
|2 fast
|0 (OCoLC)fst01423772
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|a Conference papers and proceedings.
|2 lcgft
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|a Actes de congr�es.
|2 rvmgf
|0 (CaQQLa)RVMGF-000001049
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710 |
2 |
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|a International Union of Pure and Applied Chemistry.
|b Organic Chemistry Division.
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710 |
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|a Sociedad Qu�imica de M�exico.
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776 |
0 |
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|i Print version:
|a International Symposium on the Chemistry of Natural Products (6th : 1969 : Mexico City).
|t Chemistry of natural products, 6
|z 0408700947
|w (OCoLC)274980
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856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/book/9780408700948
|z Texto completo
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880 |
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|6 505-01/(S
|a STRUCTURE ELUCIDATION OF STEROIDSAcknowledgement; References; CHAPTER 7. RECENT ADVANCES IN THE CHEMISTRY OF TERPENOID TUMOR INHIBITORS; ABSTRACT; INTRODUCTION; ISOLATION OF TUMOR-INHIBITORY PRINCIPLES FROM PLANTS; BIOLOGICAL ACTIVITY OF TUMOR-INHIBITORY PRINCIPLES; CONCLUSION; Acknowledgement; References; CHAPTER 8. ON PHOTOCHEMICAL TRANSFORMATIONS OF STEROIDS; ABSTRACT; INTRODUCTION; PHOTOCHEMICAL CYCLIZATION OF 20- AND 11-OXO STEROIDS; PHOTOCHEMICAL DECARBONYLATION OF δ5-UNSATURATED19-ALDEHYDES; PHOTOCHEMICAL TANSFORMATIONS WITH α, β-ΕΡΟΧΥ- KETONES; PHOTOSTABILIZATION; Acknowledgement.
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