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eBook Hetero Diels-Alder Methodology in Organic Synthesis, Volume 47 (Organic Chemistry) ePub

by Steven M. Weinreb,Dale L. Boger

eBook Hetero Diels-Alder Methodology in Organic Synthesis, Volume 47 (Organic Chemistry) ePub
Author: Steven M. Weinreb,Dale L. Boger
Language: English
ISBN: 0121108600
ISBN13: 978-0121108601
Publisher: Academic Press; 1 edition (November 11, 1987)
Pages: 366
Category: Medicine
Subcategory: Medical
Rating: 4.6
Votes: 471
Formats: mobi mbr txt docx
ePub file: 1743 kb
Fb2 file: 1363 kb

Organic chemistry; ) Includes index.

ACADEMIC PRESS, INC. Harcourt Brace Jovanovich, Publishers. A complete list of the books in this series can be obtained from the publisher on request. San Diego New York Berkeley Boston London Sydney Tokyo Toronto. Organic chemistry; ) Includes index. 1. Diels-Alder reaction. 2. Ring formation (Chemistry) 3. Heterocyclic compounds. I. Weinreb, Steven M. I I. Title.

Organic Chemistry: A Series of Monographs, Volume 47: Hetero Diels-Alder Methodology in Organic Synthesis focuses on the use of hetero Diels-Alder reactions as pivotal steps in natural product total syntheses.

Hardcover ISBN: 9780121108601. eBook ISBN: 9780080916972. Organic Chemistry: A Series of Monographs, Volume 47: Hetero Diels-Alder Methodology in Organic Synthesis focuses on the use of hetero Diels-Alder reactions as pivotal steps in natural product total syntheses. The publication first offers information on N-sulfinyl compounds and sulfur diimides and imino dienophiles.

Boger, Dale L. Publication date. Diels-Alder reaction, Heterocyclic compounds, Ring formation (Chemistry). 47. x, 366 p. : 24 cm. - Includes bibliographical references and index. San Diego : Academic Press. inlibrary; printdisabled; trent university;. Kahle/Austin Foundation. Bookplateleaf. Sony Alpha-A6300 (Control).

Электронная книга "Hetero Diels-Alder Methodology in Organic Synthesis", Dale L. Boger, Steven M. Weinreb. Эту книгу можно прочитать в Google Play Книгах на компьютере, а также на устройствах Android и iOS. Выделяйте текст, добавляйте закладки и делайте заметки, скачав книгу "Hetero Diels-Alder Methodology in Organic Synthesis" для чтения в офлайн-режиме.

Organic Chemistry: A Series of Monographs, Volume 47: Hetero Diels-Alder Methodology in Organic Synthesis focuses on the use of hetero Diels-Alder reactions as pivotal steps in natural . Learn how to read digital books for free.

The hetero Diels-Alder reaction is one of the most important methods for the synthesis of heterocycles. Boger DL, Weinreb SM (1987) Hetero-Diels-Alder methodology in organic synthesis. Academic Press, San DiegoGoogle Scholar. 15. Kametani T, Hibino S, (1987) In: Advances in Heterocyclic Chemistry 42:245–333Google Scholar. 16. Danishefsky SJ, De Ninno MP (1987) Angew Chem 99:15; Angew Chem Int Ed Engl 26:15CrossRefGoogle Scholar.

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Organic chemistry ;, v. 47, Organic chemistry (New York, .

Hetero Diels-Alder methodology in organic synthesis. 1 2 3 4 5. Want to Read. Are you sure you want to remove Hetero Diels-Alder methodology in organic synthesis from your list? Hetero Diels-Alder methodology in organic synthesis. Published 1987 by Academic Press in San Diego. Organic chemistry ;, v. ;, v. Classifications.

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Organic Chemistry Portal. D. L. Boger, Tetrahedron, 1983, 39, 2869. Boger, S. Weinreb, Hetero Diels-Alder Methodology in Organic Synthesis. Vol. 47, Academic Press, San Diego, 1987. Key Words: C-C BOND ENES/DIELS-ALDER REACTION/DA. Key words: n-sulfinyl/sulfur diimides/imino s/azadienes.

Organic Chemistry: A Series of Monographs, Volume 47: Hetero Diels-Alder Methodology in Organic Synthesis focuses on the use of hetero Diels-Alder reactions as pivotal steps in natural product total syntheses. The publication first offers information on N-sulfinyl compounds and sulfur diimides and imino dienophiles. Discussions focus on sulfur dioxide and related compounds, selenium dioxide, sulfur diimide cycloadditions, regiochemical, stereochemical, and mechanistic aspects, iminium salts and neutral imines, oximino compounds, and intramolecular cycloadditions. The text then takes a look at nitroso and thionitroso dienophiles and carbonyl dienophiles. The manuscript elaborates on thiocarbonyl and selenocarbonyl dienophiles and miscellaneous dienophiles. Topics include nitriles, azo compounds, selenoaldehydes, thioketones, thioesters, dithioesters, and related compounds, and thiophosgene and related compounds. The text also ponders on oxabutadienes, thiabutadienes, and azabutadienes. The publication is a valuable reference for chemists and readers interested in the Hetero Diels-Alder methodology.
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