Synthesis of 5-substituted alpha,beta-butenolides by iron-promoted intramolecular cyclocarbonylation: Addition of organometallic reagents to iron-substituted enals

Authors
Moller, C Mikulas, M Wierschem, F Ruck-Braun, K
Citation
C. Moller et al., Synthesis of 5-substituted alpha,beta-butenolides by iron-promoted intramolecular cyclocarbonylation: Addition of organometallic reagents to iron-substituted enals, SYNLETT, (2), 2000, pp. 182-184
Citations number
9
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
2
Year of publication
2000
Pages
182 - 184
Database
ISI
SICI code
0936-5214(200002):2<182:SO5ABI>2.0.ZU;2-F
Abstract
Reactions of organolithium and Grignard reagents with cyclic [eta(5)-C5H5(C O)(2)Fe]-substituted enals provide alpha,beta-butenolides by a reaction cas cade involving an intramolecular cyclocarbonylation step.