Acid-Catalyzed Cyclization of Vinylsilanes Bearing an Amino Group. Stereoselective Synthesis of Pyrrolidines1
Author:
Affiliation:
1. Department of Chemistry and Graduate School of Chemistry, University of Tsukuba, Tsukuba, Ibaraki 305-8571, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol991341o
Reference12 articles.
1. The [3 + 2] Annulation of Allylsilanes and Chlorosulfonyl Isocyanate: Stereoselective Synthesis of 2-Pyrrolidinones
2. Structural elucidation of the cyclic products formed by the reaction of 2,3--isopropylidene derivatives of -aldose with allylsilanes, vinyl ethers, or vinyl sulfides in the presence of boron trifluoride etherate
3. Diastereoselective addition of carbon electrophiles to styrylsilanes: the dimerization of .beta.-(E)-(halosilyl)styrenes
4. Silicon-directed cyclization of vinylsilanes bearing hydroxy group catalyzed by an acid
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