Enantioselective Diels–Alder Reaction of α-(Acylthio)acroleins: A New Entry to Sulfur-Containing Chiral Quaternary Carbons
Author:
Affiliation:
1. EcoTopia Science Institute, Nagoya University, Furo-cho, Chikusa, Nagoya 464-8603, Japan, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa, Nagoya 464-8603, Japan, and JST, CREST, Furo-cho, Chikusa, Nagoya 464-8603, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol300921f
Reference31 articles.
1. aIshihara, K.; Sakakura, A.InStereoselective Synthesis;Evans, P. A., Ed.Georg Thieme Verlag KG:Stuttgart, 2011; Vol.3, pp67–123.
2. Enantioselective Catalysis Based on Cationic Oxazaborolidines
3. The Diels-Alder Reaction in Total Synthesis
4. dOppolzer, W.InComprehensive Organic Synthesis;Trost, B. M.; Fleming, I., Eds.Pergamon:Oxford, 1991; Vol.5, pp315–399.
5. Design of an Organocatalyst for the Enantioselective Diels−Alder Reaction with α-Acyloxyacroleins
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