Domino reactions of vinyl malononitriles with 3-phenacylideneoxindoles for efficient synthesis of functionalized spirocyclic oxindoles.

Abstract:

:The reactions of vinyl malononitriles with 3-phenacylideneoxindoles in ethanol in the presence of DBU as base resulted in the functionalized spirocyclic oxindoles through the domino Michael addition and intramolecular nucleophilic addition to cyano group. On the other hand, the similar reaction in the presence of piperidine as base afforded the simple Michael addition products in good yields. The stereochemistry of the spirooxindoles was established with (1)H NMR data and single crystal structures.

journal_name

ACS Comb Sci

authors

Xie YJ,Sun J,Yan CG

doi

10.1021/co500006c

subject

Has Abstract

pub_date

2014-06-09 00:00:00

pages

271-80

issue

6

eissn

2156-8952

issn

2156-8944

journal_volume

16

pub_type

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