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Biomimetic Phosphate-Catalyzed Pictet-Spengler Reaction for the Synthesis of 1,1'-Disubstituted and Spiro-Tetrahydroisoquinoline Alkaloids.

Authors :
Zhao J
Méndez-Sánchez D
Ward JM
Hailes HC
Source :
The Journal of organic chemistry [J Org Chem] 2019 Jun 21; Vol. 84 (12), pp. 7702-7710. Date of Electronic Publication: 2019 May 31.
Publication Year :
2019

Abstract

Tetrahydroisoquinoline (THIQ) alkaloids are an important group of compounds that exhibit a range of bioactivities. Here, a phosphate buffer-catalyzed Pictet-Spengler reaction (PSR) using unreactive ketone substrates is described. A variety of 1,1'-disubstituted and spiro-tetrahydroisoquinoline alkaloids were readily prepared in one-step and high yields, highlighting the general applicability of this approach. This study features the role of phosphate in the aqueous-based PSR and provides an atom-efficient, sustainable route to new THIQs.

Details

Language :
English
ISSN :
1520-6904
Volume :
84
Issue :
12
Database :
MEDLINE
Journal :
The Journal of organic chemistry
Publication Type :
Academic Journal
Accession number :
31095375
Full Text :
https://doi.org/10.1021/acs.joc.9b00527