Syntheses of chiral 1,3-disubstituted tetrahydro-β-carbolines via CIAT process: highly stereoselective Pictet–Spengler reaction of d-tryptophan ester hydrochlorides with various aldehydes-Reference-Cited by-同舟云学术

Syntheses of chiral 1,3-disubstituted tetrahydro-β-carbolines via CIAT process: highly stereoselective Pictet–Spengler reaction of d-tryptophan ester hydrochlorides with various aldehydes

Published:2009-03 Issue:4 Volume:20 Page:430-439
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Xiao Sen,Lu Xia,Shi Xiao-Xin,Sun Yu,Liang Li-Li,Yu Xin-Hong,Dong Jing

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference56 articles.

1. Highly Enantioselective Catalytic Acyl-Pictet−Spengler Reactions

2. Catalytic Asymmetric Pictet–Spengler Reactions via Sulfenyliminium Ions

3. Diasteroselective Cyclizations with Enantiopure Malonaldehyde Monocycloacetals

4. Strictosidine Synthase: Mechanism of a Pictet−Spengler Catalyzing Enzyme

5. 1-Substituted β-Carbolines by a Pictet−Spengler Cyclization with Thioortho Esters and Carbon−Carbon Bond Formation via N-Sulfonyl Iminium Ions Generated from N,S-Sulfonyl Acetals

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