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Synthesis of novel spiroazetidinones by selective lactam‐carbonyl cleavage in 1‐aryl/cyclohexyl‐3,3‐diphenyl‐1′‐(diphenylacetyl)spiro[azetidin‐2,3′‐indoline]‐2′,4‐diones
Author(s) -
Singh Girija S.
Publication year - 2000
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570370556
Subject(s) - chemistry , isatin , indoline , cleavage (geology) , aryl , lactam , sodium hydroxide , ethanol , medicinal chemistry , stereochemistry , organic chemistry , alkyl , geotechnical engineering , fracture (geology) , engineering
Titled compounds undergo selective N‐C cleavage on treatment with sodium hydroxide in ethanol affording a series of novel isatin‐based spiroazetidinones.