Unprecedented Stereocontrol in the Synthesis of 1,2,3-Trisubstituted Tetrahydro-β-carbolines through an Asymmetric Pictet-Spengler Reaction towards Sarpagine-Type Indole Alkaloids-Reference-Cited by-同舟云学术

Unprecedented Stereocontrol in the Synthesis of 1,2,3-Trisubstituted Tetrahydro-β-carbolines through an Asymmetric Pictet-Spengler Reaction towards Sarpagine-Type Indole Alkaloids

Published:2018-06-21 Issue:24 Volume:2018 Page:3224-3229
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Rahman M. Toufiqur¹^ORCID,Cook James M.¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry; University of Wisconsin-Milwaukee; 3210 N Cramer Street 53211 Milwaukee WI- USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201800600/fullpdf

Reference59 articles.

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

2. The Chiral Pool in the Pictet–Spengler Reaction for the Synthesis of β-Carbolines

3. The Pictet-Spengler Reaction Still on Stage

4. The intermolecular Pictet-Spengler condensation with chiral carbonyl derivatives in the stereoselective syntheses of optically-active isoquinoline and indole alkaloids

5. Application of Pictet–Spengler Reaction to Indole-Based Alkaloids Containing Tetrahydro-β-carboline Scaffold in Combinatorial Chemistry

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