MUKAIYAMA ALDOL REACTIONS OF PI-ALLYLTRICARBONYLIRON LACTONE AND LACTAM COMPLEXES BEARING TRIMETHYLSILYL ENOL ETHER SIDE-CHAINS - NOT JUST FORMAL, BUT GENUINE 1,7 INDUCTION OF CHIRALITY

Authors
LEY SV COX LR MIDDLETON B WORRALL JM
Citation
Sv. Ley et al., MUKAIYAMA ALDOL REACTIONS OF PI-ALLYLTRICARBONYLIRON LACTONE AND LACTAM COMPLEXES BEARING TRIMETHYLSILYL ENOL ETHER SIDE-CHAINS - NOT JUST FORMAL, BUT GENUINE 1,7 INDUCTION OF CHIRALITY, Chemical communications, (13), 1998, pp. 1339-1340
Citations number
10
Categorie Soggetti
Chemistry
Journal title
Chemical communications → ACNP
ISSN journal
13597345
Issue
13
Year of publication
1998
Pages
1339 - 1340
Database
ISI
SICI code
1359-7345(1998):13<1339:MAROPL>2.0.ZU;2-G
Abstract
A comparison of diastereoselectivities in the Mukaiyama aldol reaction s of three types of trimethylsilyl enol ether substituted iron carbony l complexes has provided evidence for the stereodirecting effect of re mote substituents in pi-allyltricarbonyliron lactone and lactam comple xes.