Organocatalytic Enantioselective Michael–Michael–Henry Reaction Cascade. An Entry to Highly Functionalized Hajos–Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons-Reference-Cited by-同舟云学术

Organocatalytic Enantioselective Michael–Michael–Henry Reaction Cascade. An Entry to Highly Functionalized Hajos–Parrish-Type Ketones with Five to Six Contiguous Stereogenic Centers and Two Quaternary Carbons

Published:2016-03-28 Issue:8 Volume:18 Page:1760-1763
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Raja Arun¹,Hong Bor-Cherng¹,Liao Ju-Hsiou¹,Lee Gene-Hsiang²

Affiliation:

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

2. Department of Chemistry, National Taiwan University, Taipei 106, Taiwan, R.O.C.

Funder

Ministry of Science and Technology, Taiwan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b00459

Reference40 articles.

1. Catalytic C–C Bond-Forming Multi-Component Cascade or Domino Reactions: Pushing the Boundaries of Complexity in Asymmetric Organocatalysis

2. Recent Advances in Organocatalytic Methods for Asymmetric CC Bond Formation

3. New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures

4. Asymmetric synthesis of bicyclic intermediates of natural product chemistry

5. The Wieland-Miescher Ketone: A Journey from Organocatalysis to Natural Product Synthesis

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