Thiophenol-mediated improvement of the Pictet–Spengler cyclization of N-tosyl-β-phenethylamines with aldehydes-Reference-Cited by-同舟云学术

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Thiophenol-mediated improvement of the Pictet–Spengler cyclization of N-tosyl-β-phenethylamines with aldehydes

Published:2006-10 Issue:43 Volume:47 Page:7545-7549
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Silveira Claudio C.,Vieira Adriano S.,Kaufman Teodoro S.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. The Pictet–Spengler Synthesis of Tetrahydroisoquinolines and Related Compounds;Whaley,1951

2. The Pictet-Spengler condensation: a new direction for an old reaction

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2. Tetrahydroisoquinolines;Privileged Structures in Drug Discovery;2018-03-09

3. Lewis acid promoted three-component reactions of aziridines, arenes and aldehydes: an efficient and diastereoselective synthesis of cis-1,4-disubstituted tetrahydroisoquinolines;Tetrahedron;2015-09

4. Mild and efficient cyanuric chloride catalyzed Pictet–Spengler reaction;Beilstein Journal of Organic Chemistry;2013-06-26

5. Synthesis, cytotoxicity and QSAR study of N-tosyl-1,2,3,4-tetrahydroisoquinoline derivatives;Archives of Pharmacal Research;2013-04-21

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