Tandem ene addition/Diels-Alder cycloaddition reactions of methyl linoleate with 4-phenyl-1,2,4-triazoline-3,5-dione and diethyl azodicarboxylate

Authors
McLellan, JF Mortier, RM Orszulike, ST Paton, RM
Citation
Jf. Mclellan et al., Tandem ene addition/Diels-Alder cycloaddition reactions of methyl linoleate with 4-phenyl-1,2,4-triazoline-3,5-dione and diethyl azodicarboxylate, J CHEM R-S, (7), 2000, pp. 339-341
Citations number
8
Categorie Soggetti
Chemistry
Journal title
JOURNAL OF CHEMICAL RESEARCH-S
ISSN journal
03082342 → ACNP
Issue
7
Year of publication
2000
Pages
339 - 341
Database
ISI
SICI code
0308-2342(200007):7<339:TEACRO>2.0.ZU;2-1
Abstract
Treatment of methyl linoleate with 4-phenyl-1,2,4-triazoline-3,5-dione affo rds 1:1 adducts resulting from ene addition, and 1:2 adducts formed by ene addition followed by Diels Alder cycloaddition. The corresponding reaction of diethyl azodicarboxylate yields predominantly 1:1 ene products.