Studies on diastereoselectivity of the cobalt(I) catalyzed cycloisomerization of substituted ε-acetylenic β-ketoester
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Stereoselective access to the basic skeleton of tetracyclic diterpenes via a sequence of consecutive [3 + 2], [2 + 2 + 2], and [4 + 2] cycloaddition reactions
2. Synthetic approach to aphidicolan and stemodan basic skeletons using a “Tandem Principle” [2+2+2] and [4+2] cycloaddition reactions
3. New Cobalt Catalyzed Cycloisomerization of β-Ketoester ε-Acetylenic
4. Intramolecular ene approach to stereocontrol over three contiguous chiral centers
5. Cyclization of olefinic β-ketoesters. A novel synthesis of Δ8(14)-podocarpen-13-one
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1. Cobalt-Catalysed C-C Bond Formation and [2+2+2] Annulation of 1,3-Dicarbonyls to Terminal Alkynes;European Journal of Organic Chemistry;2019-06-18
2. Alkylation and Acylation of Aldehydes, Ketones, and Their Derivatives;Comprehensive Organic Transformations;2018-02-28
3. Development of an enantioselective amine–silver co-catalyzed Conia-ene reaction;Chemical Communications;2017
4. Catalytic Conia-ene and related reactions;Chemical Society Reviews;2015
5. Reactions of acetylenes in superbasic media. Recent advances;Russian Chemical Reviews;2014-07-24
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