Journal ArticleDOI
Total synthesis of gibberellic acid. A simple synthesis of a key intermediate
E. J. Corey,John E. Munroe +1 more
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This article is published in Journal of the American Chemical Society.The article was published on 1982-11-01. It has received 70 citations till now. The article focuses on the topics: Gibberellic acid & Total synthesis.read more
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Journal ArticleDOI
Catalytic enantioselective Diels--Alder reactions: methods, mechanistic fundamentals, pathways, and applications.
TL;DR: Research by this group on the development and understanding of enantioselective versions of the Diels-Alder reactions is described, based on presentations given first at the University of Cologne, Germany, then at the Roger Adams Award Symposium, and later at the Bürgenstock Conference of 2001.
Journal ArticleDOI
Katalytische enantioselektive Diels-Alder-Reaktionen: Methoden, mechanistische Grundlagen, Reaktionswege und Anwendungen
TL;DR: In this paper, Alder-Alder-Reaktion has been studied in der ganzen Welt, e.g. in the field of chemical engineering, and a number of experiments have been carried out.
Journal ArticleDOI
Synthesis of Functionalized Bicyclo[3.2.1]octanes and Their Multiple Uses in Organic Chemistry.
TL;DR: It is shown here how ring closure of the Two-Carbon Bridge and Ring Expansion of Bicyclo[2.2.1]heptanes and Fragmentations Leading to Nonbridged Carbocycles 63 leading to Reactivity 63 can be modelled.
Book ChapterDOI
7.2 – Claisen Rearrangements
TL;DR: In this paper, a survey of variants of the Claisen rearrangement that are of general use in stereoselective organic synthesis is presented, highlighting the influence of steric and electronic parameters on transition state geometries.
Reference EntryDOI
Organocopper Reagents: Substitution, Conjugate Addition, Carbo/Metallocupration, and Other Reactions
TL;DR: In this paper, two reviews were contributed to the Organic Reactions series covering substitution and conjugate addition reactions in organocopper chemistry, and many solutions to this problem now exist.