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Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates

D. A. Evans, +2 more
- 01 Apr 1981 - 
- Vol. 103, Iss: 29, pp 2127-2129
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This article is published in Journal of the American Chemical Society.The article was published on 1981-04-01. It has received 1282 citations till now. The article focuses on the topics: Aldol reaction & Enantioselective synthesis.

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Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions.

TL;DR: The motivation for studying Pd-catalyzed C-H functionalization assisted by weakly coordinating functional groups is discussed, and efforts to bring reactions of this type to fruition are chronicle.
Journal ArticleDOI

Transition metal-catalyzed C–H activation reactions: diastereoselectivity and enantioselectivity

TL;DR: This critical review discusses historical and contemporary research in the field of transition metal-catalyzed carbon-hydrogen (C-H) bond activation through the lens of stereoselectivity, placing an emphasis on reactions that are (or may soon become) relevant in the realm of organic synthesis.
Journal ArticleDOI

Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis

TL;DR: In this article, it is shown that double asymmetric induction can be analyzed in terms of the single asymmetric reactions of each of the two chiral reactants, and a new strategy based on this rule for the predictable creation of new chiral centers is discussed and the use of this strategy for the synthesis of sugars and macrolides is presented.
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