Sequential Asymmetric Catalysis in Michael–Michael–Michael–Aldol Reactions: Merging Organocatalysis with Photoredox Catalysis in a One-Pot Enantioselective Synthesis of Highly Functionalized Decalines Bearing a Quaternary Carbon Stereocenter-Reference-Cited by-同舟云学术

Sequential Asymmetric Catalysis in Michael–Michael–Michael–Aldol Reactions: Merging Organocatalysis with Photoredox Catalysis in a One-Pot Enantioselective Synthesis of Highly Functionalized Decalines Bearing a Quaternary Carbon Stereocenter

Published:2013-11-23 Issue:24 Volume:15 Page:6258-6261
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Hong Bor-Cherng¹,Lin Cheng-Wei¹,Liao Wei-Kai¹,Lee Gene-Hsiang¹

Affiliation:

1. Department of Chemistry and Biochemistry, National Chung Cheng University, Chia-Yi, 621, Taiwan, R.O.C., and Instrumentation Center, National Taiwan University, Taipei, 106, Taiwan, R.O.C.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol403113c

Reference56 articles.

1. Visible Light Photocatalysis: The Development of Photocatalytic Radical Ion Cycloadditions

2. Photoredox functionalization of C–H bonds adjacent to a nitrogen atom

3. Visible-Light Photoredox Catalysis

4. Visible light photoredox catalysis: applications in organic synthesis

5. Visible light photocatalysis as a greener approach to photochemical synthesis

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