ELECTRONIC VERSUS STERIC EFFECTS IN 5-ENDO-TRIG-LIKE ELECTROPHILIC CYCLIZATIONS

Authors
LANDAIS Y PLANCHENAULT D
Citation
Y. Landais et D. Planchenault, ELECTRONIC VERSUS STERIC EFFECTS IN 5-ENDO-TRIG-LIKE ELECTROPHILIC CYCLIZATIONS, Synlett, (11), 1995, pp. 1191
Citations number
27
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
11
Year of publication
1995
Database
ISI
SICI code
0936-5214(1995):11<1191:EVSEI5>2.0.ZU;2-Q
Abstract
Electronically and sterically differentiated allylic substituents such as RO, NHPh, PhS, and PhSO(2) groups have been used to demonstrate th e influence of electronic and/or steric effects in the stereocontrol o f electrophilic 5-endo-trig-like cyclizations of 2-substituted-3-alken ols.