TRIMETHYLSILYL DERIVATIVES AS FINAL NUCLEOPHILES IN THE TANDEM SEQUENCE OF AN ARSCL-INITIATED AD(E) REACTION RESULTING IN THE SYNTHESIS OF POLYFUNCTIONAL COMPOUNDS

Authors
HAYFORD A LOVDAHL M LAZAREVA MI KRYSCHENKO YK JOHNSON T DILMAN AD SMOLIAKOVA IP CAPLE R SMIT WA
Citation
A. Hayford et al., TRIMETHYLSILYL DERIVATIVES AS FINAL NUCLEOPHILES IN THE TANDEM SEQUENCE OF AN ARSCL-INITIATED AD(E) REACTION RESULTING IN THE SYNTHESIS OF POLYFUNCTIONAL COMPOUNDS, Mendeleev communications, (2), 1997, pp. 48-50
Citations number
9
Categorie Soggetti
Chemistry
Journal title
Mendeleev communications → ACNP
ISSN journal
09599436
Issue
2
Year of publication
1997
Pages
48 - 50
Database
ISI
SICI code
0959-9436(1997):2<48:TDAFNI>2.0.ZU;2-C
Abstract
The use of allyl silanes and silyl vinyl ethers in the final step of a Lewis acid-mediated sequence involving reaction of ArSCl, two vinyl e ther units and a C-nucleophile has been studied, thereby allowing intr oduction of functional groups into the four-component adduct.