Enantioselective [4 + 2] Cycloaddition of o-Quinone Methides and Vinyl Sulfides: Indirect Access to Generally Substituted Chiral Chromanes
Author:
Affiliation:
1. Department of Chemistry, the Hong Kong University of Science and Technology (HKUST), Clear Water Bay, Kowloon, Hong Kong SAR, China
Funder
Research Grants Council, University Grants Committee
Shenzhen Science and Technology Innovation Committee
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b00867
Reference65 articles.
1. Hetero Diels–Alder reaction of olefin with o-quinone methides generated using (±)-binolphosphoric acid for the stereoselective synthesis of 2,4-diarylbenzopyrans: application to the formal synthesis of myristinin B/C
2. Asymmetric synthesis of chiral chromans
3. Syntheses of chromenes and chromanesvia o-quinone methide intermediates
4. Natural and Synthetic Chromenes, Fused Chromenes, and Versatility of Dihydrobenzo[h]chromenes in Organic Synthesis
5. Catalytic Synthesis of 2H-Chromenes
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