Efforts Directed Toward the Total Synthesis of Ikarugamycin PDF Download
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Author: Ronald Isamu Sato
Publisher:
ISBN:
Category :
Languages : en
Pages : 234
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Book Description
Author: Ronald Isamu Sato
Publisher:
ISBN:
Category :
Languages : en
Pages : 234
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Book Description
Author: Anthony J. Thomas
Publisher:
ISBN:
Category :
Languages : en
Pages : 240
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Author: Michael Joseph O'Brien
Publisher:
ISBN:
Category :
Languages : en
Pages : 420
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Author: Charles Harry Weidner
Publisher:
ISBN:
Category :
Languages : en
Pages : 808
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Author:
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Category : Dissertation abstracts
Languages : en
Pages : 800
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Category : Dissertations, Academic
Languages : en
Pages : 754
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Author: Leo A. Paquette
Publisher: John Wiley & Sons
ISBN: 9780470856253
Category : Science
Languages : en
Pages : 618
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Book Description
Derived from the renowned, Encyclopedia of Reagents for Organic Synthesis (EROS), the related editors have created a new handbook which focuses on chiral reagents used in asymmetric synthesis and is designed for the chemist at the bench. This new handbook follows the same format as the Encyclopedia, including an introduction and an alphabetical arrangement of the reagents. As chiral reagents are the key for the successful asymmetric synthesis, choosing the right reagents is essential, in this handy reference the editors give details on how to prepare, store and use the reagents as well as providing key reactions to demonstrate where reagents have been successfully used. Comprehensive information on 226 reagents Covers 64 reagents which were not included in EROS All information in one easy to use volume – at an affordable price All reagents included will be added to e-EROS – please visit the site where you can gain access to over 50,000 reactions and 3,800 of the most frequently consulted reagents. Visit: www.interscience.wiley.com/eros
Author: Scott A. Frank
Publisher:
ISBN:
Category :
Languages : en
Pages : 432
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Category : Dissertations, Academic
Languages : en
Pages : 770
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Author: Dennis G. Hall
Publisher: John Wiley & Sons
ISBN: 0470436905
Category : Science
Languages : en
Pages : 624
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Book Description
Allylic boron compounds have gained a prominent position as a truly practical class of synthetic reagents in the past twenty-five years. Their main application as a method for the stereoselective synthesis of homoallylic alcohols by allyl-transfer to carbonyl compounds is essentially unmatched. In this process, a new carbon-carbon bond is formed, and up to two new stereogenic centers are created in a predictably controlled manner. Highly effective and general enantioselective variants are available, with countless applications in the total syntheses of polyacetate and polypropionate natural products. Furthermore, the residual allylic unit can be manipulated through a number of different transformations such as oxidative cleavage, olefin metathesis, hydrometalations, and many others. The discovery of Lewis and Brønsted acid catalyzed manifolds recently, has opened new doors for further development of this important reaction. This book provides an up-to-date, comprehensive survey of the literature of this rich chemistry as it pertains to organic synthesis. Consistent with the goal of Organic Reactions, the content and presentation emphasize the preparative aspects of the reactions, giving considerable attention to the scope and limitations of the individual transformations along with detailed experimental procedures. A tabular survey of all examples of carbonyl allylboration used in organic synthesis is presented in nine tables organized by type of allylic boron reagent with listings within each table according to increasing carbon number of the carbonyl substrates. The literature is covered through December 2010, including a new listing of nearly 200 literature citations that supplement the original coverage of 834 references used in the earlier hard cover version of the chapter. Allylboration of Carbonyl Compounds is intended to be a useful, easily read reference book for all practitioners of synthetic organic chemistry working in academic and industrial laboratories.
