Organocatalytic [4 + 2] cyclocondensation of α,β-unsaturated acyl chlorides with imines: highly enantioselective synthesis of dihydropyridinone and piperidine derivatives-Reference-Cited by-同舟云学术

Organocatalytic [4 + 2] cyclocondensation of α,β-unsaturated acyl chlorides with imines: highly enantioselective synthesis of dihydropyridinone and piperidine derivatives

Published:2014 Issue:14 Volume:12 Page:2167
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Jia Wen-Qiang,Chen Xiang-Yu,Sun Li-Hui,Ye Song

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB00114A

Reference28 articles.

1. Catalytic Asymmetric Formation of δ-Lactones by [4+2] Cycloaddition of Zwitterionic Dienolates Generated from α,β-Unsaturated Acid Chlorides

2. Lewis Acid−Lewis Base Catalyzed Enantioselective Hetero-Diels−Alder Reaction for Direct Access to δ-Lactones

3. Catalytic Asymmetric Formation of δ-Lactones from Unsaturated Acyl Halides

4. N-Heterocyclic Carbene-Catalyzed Cyclization of Unsaturated Acyl Chlorides and Ketones

5. Highly Enantioselective γ-Amination of α,β-Unsaturated Acyl Chlorides with Azodicarboxylates: Efficient Synthesis of Chiral γ-Amino Acid Derivatives

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