UNUSUAL FORMATION OF VINYL ETHER DERIVATIVES IN THE REACTION OF TRIBUTYLTIN HYDRIDE WITH FISCHER CARBENE COMPLEXES ANCHORED ON A CHALCOGEN-STABILIZED IRON CARBONYL CLUSTER

Citation
P. Mathur et al., UNUSUAL FORMATION OF VINYL ETHER DERIVATIVES IN THE REACTION OF TRIBUTYLTIN HYDRIDE WITH FISCHER CARBENE COMPLEXES ANCHORED ON A CHALCOGEN-STABILIZED IRON CARBONYL CLUSTER, Organometallics, 16(26), 1997, pp. 6028-6031
Citations number
24
Journal title
ISSN journal
02767333
Volume
16
Issue
26
Year of publication
1997
Pages
6028 - 6031
Database
ISI
SICI code
0276-7333(1997)16:26<6028:UFOVED>2.0.ZU;2-2
Abstract
Treatment of Fe-2(CO)(6){mu-EC(Ph)=C(E')-[C(OEt)=M(CO)(5)]} (1: E, E' = Se; M = Cr. 2: E, E' = Se; M = W. 3: E = S; E' = Te; M = W) with exc ess Bu3SnH in hexane at 0 degrees C produces enol ether derivatives: ( CO)(6)Fe-2{mu-EC(Ph)(H)-C(E')=C(H)(OEt)} ((Z)-4a: E, E' = Se. (E)-4b: E, E' = Se. (Z)-5a: E = S; E' = Te. (E)-5b: E = S; E' = Te). For E, E' = Se, using 1 equiv of Bu3SnH, the alpha-alkoxyallylstannane complex, (CO)(6)Fe-2{mu-Se(Ph)C=C(Se)-C(OEt)(H)SnBu3} (6), was isolated. The m olecular structure of (E)-4b was confirmed by X-ray analysis.