Asymmetric Methallylation of Ketones Catalyzed by a Highly Active Organocatalyst 3,3′-F2-BINOL-Reference-Cited by-同舟云学术

Asymmetric Methallylation of Ketones Catalyzed by a Highly Active Organocatalyst 3,3′-F2-BINOL

Published:2013-03-25 Issue:7 Volume:15 Page:1710-1713
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhang Yongda¹,Li Ning¹,Qu Bo¹,Ma Shengli¹,Lee Heewon¹,Gonnella Nina C.¹,Gao Joe¹,Li Wenjie¹,Tan Zhulin¹,Reeves Jonathan T.¹,Wang Jun¹,Lorenz Jon C.¹,Li Guisheng¹,Reeves Diana C.¹,Premasiri Ajith¹,Grinberg Nelu¹,Haddad Nizar¹,Lu Bruce Z.¹,Song Jinhua J.¹,Senanayake Chris H.¹

Affiliation:

1. Department of Chemical Development, Boehringer Ingelheim Pharmaceuticals, Inc., 900 Ridgebury Road/P.O. Box 368, Ridgefield, Connecticut 06877-0368, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol400498a

Reference30 articles.

1. Catalytic Enantioselective Allylation of Carbonyl Compounds and Imines

2. The Domino Multicomponent Allylation Reaction for the Stereoselective Synthesis of Homoallylic Alcohols

3. Catalytic Asymmetric Methallylation of Ketones with an (H8-BINOLate)Ti-Based Catalyst

4. Asymmetric Synthesis of 2°- and 3°-Carbinols via B-Methallyl-10-(TMS and Ph)-9-borabicyclo[3.3.2]decanes

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