Highly Enantio- and Diastereoselective Vinylogous Aldol Reaction by LiCl-Assisted BINOL–Titanium Species
Author:
Affiliation:
1. State Key Laboratory of Fine Chemicals, School of Pharmaceutical Science and Technology, Faculty of Chemical, Environmental and Biological Science and Technology, Dalian University of Technology, Dalian 116023, P. R. China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol300946j
Reference69 articles.
1. The Vinylogous Aldol Reaction: A Valuable, Yet Understated Carbon−Carbon Bond-Forming Maneuver
2. Recent Advances in Asymmetric Aldol Reaction of Masked Acetoacetic Esters Promoted by Ti(IV) / BINOL: A New Methodology, Non-Linear Effects and Autoinduction
3. Catalytic, Enantioselective, Vinylogous Aldol Reactions
4. The Vinylogous Aldol and Related Addition Reactions: Ten Years of Progress
5. The Organocatalytic Vinylogous Aldol Reaction: Recent Advances
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