Thioorthoesters in the activated Pictet–Spengler cyclization. Synthesis of 1-thiosubstituted tetrahydroisoquinolines and carboncarbon bond formation via sulfonyl iminium ions generated from N,S-sulfonyl acetals-Reference-Cited by-同舟云学术

Thioorthoesters in the activated Pictet–Spengler cyclization. Synthesis of 1-thiosubstituted tetrahydroisoquinolines and carboncarbon bond formation via sulfonyl iminium ions generated from N,S-sulfonyl acetals

Published:2003-08 Issue:32 Volume:44 Page:6137-6140
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Silveira Claudio C,Bernardi Carmem R,Braga Antonio L,Kaufman Teodoro S

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference43 articles.

1. Development of a strategy for synthesis of the unusual marine alkaloid sarain A

2. A new approach to piperidine alkaloids: an enantioselective total synthesis of (2S,6R)- and (2R,6S)-dihydropinidine

3. A short and enantioselective synthesis of (+)-Anatoxin-a

4. A tosyliminium ion-based total synthesis of (±)-schefferine

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