Issue 11, 2016

Silver(i)-catalysed domino alkyne-annulation/Diels–Alder reaction: a mild synthetic approach to tetrahydrospiro[carbazole-4,3′-indoline] scaffolds

Abstract

A mild and efficient AgOTf catalyzed alkyne-annulation/Diels–Alder cascade for the construction of tetrahydrospiro[carbazole-4,3′-indoline] derivatives has been established from N-tosyl-2-(but-3-en-1-yn-1-yl) aniline in the presence of methyleneindolinones. This strategy provides access to the one-pot synthesis of a new class of various novel and structurally complex spirooxindole molecules with high diastereoselectivity.

Graphical abstract: Silver(i)-catalysed domino alkyne-annulation/Diels–Alder reaction: a mild synthetic approach to tetrahydrospiro[carbazole-4,3′-indoline] scaffolds

Supplementary files

Article information

Article type
Research Article
Submitted
03 Aug 2016
Accepted
02 Sep 2016
First published
05 Sep 2016

Org. Chem. Front., 2016,3, 1503-1508

Silver(I)-catalysed domino alkyne-annulation/Diels–Alder reaction: a mild synthetic approach to tetrahydrospiro[carbazole-4,3′-indoline] scaffolds

P. Sharma, N. P. Kumar, N. H. Krishna, D. Prasanna, B. Sridhar and N. Shankaraiah, Org. Chem. Front., 2016, 3, 1503 DOI: 10.1039/C6QO00430J

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