Indole and Biogenetically Related Alkaloids PDF Download
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Author: John David Phillipson
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 404
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Book Description
Author: John David Phillipson
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 404
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Book Description
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
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Book Description
Author: W. I. Taylor
Publisher: Elsevier
ISBN: 1483221741
Category : Science
Languages : en
Pages : 162
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Book Description
A Course in Organic Chemistry Advanced Section, Volume 27: Indole Alkaloids: An Introduction to the Enamine Chemistry of Natural Products describes the chemistry of selected alkaloids that contain indolic or closely related nuclei. Some five hundred of these compounds have been obtained from about three hundred plants mostly of the family Apocynaceae. This book is composed of 12 chapters that specifically cover the chemistry of the complex indoles. The introductory chapters deal with the origin, isolation, characterization, basic chemistry, and simple derivatives of indole alkaloids. The remaining chapters examine the biogenesis, basic chemistry, stereochemistry, and structure of selected complex alkaloids of various origins. These chapters include tetrahydro-?-carboline, strychnos, iboga, picralima, and eburnamine alkaloids, cinchonamine, quinamine, and ajmaline-sarpagine bases. This text is of great value to organic chemists and researchers.
Author: Hans-Joachim Knolker
Publisher: Academic Press
ISBN: 0128209836
Category : Science
Languages : en
Pages : 254
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Book Description
The Alkaloids, Volume 83, is the newest release in a series that has covered the topic for more than 60 years. As the esteemed, leading reference in the field of alkaloid chemistry, this series covers all aspects of alkaloids, including their chemistry, biology and pharmacology. Sections are presented as high-quality, timeless reviews written by renowned experts in the field. New chapters in this release include Lamellarin alkaloids: Isolation, synthesis, and biological activity, Chemodiversity, chemotaxonomy and chemoecology of Amaryllidaceae alkaloids, and The indole-based subincanadine alkaloids and their biogenetic congeners. - Provides the latest information on the study of alkaloids - Covers their chemistry, biology, pharmacology and medical applications - Contains more than 70 published volumes in this interesting field of study
Author: William I. Taylor
Publisher: Pergamon
ISBN:
Category : Science
Languages : en
Pages : 170
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Book Description
Author: Atta-ur- Rahman
Publisher: Oxford University Press, USA
ISBN:
Category : Language Arts & Disciplines
Languages : en
Pages : 288
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Book Description
Author: R. H. Manske
Publisher:
ISBN: 9780124695085
Category : Alkaloids
Languages : en
Pages : 861
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Author: John Clark Lorenz
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Author: Ishac Dib Nasri
Publisher:
ISBN:
Category : Alkaloids
Languages : en
Pages : 142
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Book Description
Author: Seyed Mohammad Nabavi
Publisher: Elsevier
ISBN: 0128175192
Category : Science
Languages : en
Pages : 880
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Book Description
Recent Advances in Natural Products Analysis is a thorough guide to the latest analytical methods used for identifying and studying bioactive phytochemicals and other natural products. Chemical compounds, such as flavonoids, alkaloids, carotenoids and saponins are examined, highlighting the many techniques for studying their properties. Each chapter is devoted to a compound category, beginning with the underlying chemical properties of the main components followed by techniques of extraction, purification and fractionation, and then techniques of identification and quantification. Biological activities, possible interactions, levels found in plants, the effects of processing, and current and potential industrial applications are also included. Focuses on the latest analytical techniques used for studying phytochemical and other biological compounds Authored and edited by the top worldwide experts in their field Discusses the current and potential applications and predicts future trends of each compound group
