Cyclopropenation of Alkylidene Carbenes Derived from α-Silyl Ketones
Author:
Affiliation:
1. Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607-7061
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja101998w
Reference43 articles.
1. aTaber, D. F.InMethods of Organic Chemistry,4th ed.Helmchen, G., Ed.Georg Thieme Verlag:New York, 1995; Vol.E21, p1127.
2. Alkylidenecarbenes, Alkylidenecarbenoids, and Competing Species: Which Is Responsible for Vinylic Nucleophilic Substitution, [1 + 2] Cycloadditions, 1,5-CH Insertions, and the Fritsch−Buttenberg−Wiechell Rearrangement?
3. Stereoelectronic Effect for the Selectivity in C−H Insertion of Alkylidene Carbenes and Its Application to the Synthesis of Platensimycin
4. Synthesis of α-Necrodol: Unexpected Formation of a Cyclopropene
5. Enantiomerically Enriched Cyclopropene Derivatives: Versatile Building Blocks in Asymmetric Synthesis
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