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Diastereoselective synthesis of γ‐dispiroiminolactone bearing naphthalene or bipyridine pendant groups
Author(s) -
Maghsoodlou Malek T.,
Hazeri Nourollah,
HabibiKhorassani Sayyed M.,
Ziyaadini Morteza,
Marandi Ghasem,
KhandanBarani Khatereh,
Ebrahimi Pouneh,
Charati Faramarz Rostami,
Sobolev Alexandre,
Makha Mohamed
Publication year - 2009
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.164
Subject(s) - chemistry , naphthalene , condensation , bipyridine , condensation reaction , organic chemistry , polymer chemistry , medicinal chemistry , stereochemistry , catalysis , crystal structure , physics , thermodynamics
AbstractDiastereoselective γ‐dispiroiminolactone products 4a , 4b , 4c , 4d , 4e , 4f , 4g , 4h , 4i , 4j , 4k , 4l , 4m were obtained from a condensation of the highly reactive 1:1 intermediate of isocyanides and acetylenic esters with aromatic α‐dicarbonyls compounds 3a, b . J. Heterocyclic Chem., (2009).