Issue 36, 2020

Synthesis of 1-benzylisoindoline and 1-benzyl-tetrahydroisoquinoline through nucleophilic addition of organozinc reagents to N,O-acetals

Abstract

A new approach to access 1-benzylisoindoline and 1-benzyl-tetrahydroisoquinoline has been developed through nucleophilic addition of organozinc reagents to N,O-acetals. A number of substituted organozinc reagents were amenable for this transformation, and the desired products were obtained with excellent yields. Moreover, Sc(OTf)3 proved to be an effective catalyst for the formation of 1-benzylisoindoline and 1-benzyl-tetrahydroisoquinoline using such nucleophilic addition.

Graphical abstract: Synthesis of 1-benzylisoindoline and 1-benzyl-tetrahydroisoquinoline through nucleophilic addition of organozinc reagents to N,O-acetals

Supplementary files

Article information

Article type
Paper
Submitted
17 Jul 2020
Accepted
01 Sep 2020
First published
01 Sep 2020

Org. Biomol. Chem., 2020,18, 7139-7150

Synthesis of 1-benzylisoindoline and 1-benzyl-tetrahydroisoquinoline through nucleophilic addition of organozinc reagents to N,O-acetals

R. Ma, J. Sun, C. Liu, L. Chen, C. Si and B. Wei, Org. Biomol. Chem., 2020, 18, 7139 DOI: 10.1039/D0OB01477J

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