Rhodium-mediated cyclopentane construction can compete with .beta.-hydride elimination: synthesis of (.+-.)-tochuinyl acetate
摘要:
Rhodium(II) carboxylate catalyzed C-H insertion to form a cyclopentane is shown to compete effectively with beta-hydride elimination, except when the beta-hydrogen is ternary. Cyclization of diazo ester 27 gives 28, which is converted in three steps to (+/-)-tochuinyl acetate 25. Both the cyclization to form 28 and the alkylation of 28 proceed with remarkable diastereoselectivity.
4-<i>Endo</i>-<i>T</i><i>rig</i> Cyclization Processes Using Bis(collidine)bromine(I) Hexafluorophosphate as Reagent: Preparation of 2-Oxetanones, 2-Azetidinones, and Oxetanes
作者:Fadi Homsi、Gérard Rousseau
DOI:10.1021/jo9810361
日期:1999.1.1
Reaction in methylene chloride of bis(collidine)bromine(I) hexafluorophosphate with alpha,beta-unsaturated acids and alpha,beta-unsaturated N-sulfonamides was found to lead diastereospecifically to the corresponding 2-oxetanones and 2-azetidinones in moderate yields (23-60%), by an almost unknown 4-endo cyclization. This process allow the synthesis of these interesting classes of products in one step
A new procedure for Horner-Wadsworth-Emmons olefination of carbonyl compounds
作者:Francesco Bonadies、Antonella Cardilli、Alessandra Lattanzi、Liliana R. Orelli、Arrigo Scettri
DOI:10.1016/s0040-4039(00)76914-0
日期:1994.5
aldehydes undergo an efficient E-stereoselective Horner-Wadsworth-Emmonsolefination by generation of phosphonate carbanion with lithium hydroxide. The reaction proceeds satisfactorily with linear, cyclic, polifunctional ketones in the presence of activated zeolites and and by the slow addition of the base.
Rhodium-mediated cyclopentane construction can compete with .beta.-hydride elimination: synthesis of (.+-.)-tochuinyl acetate
作者:Douglass F. Taber、Michael J. Hennessy、James P. Louey
DOI:10.1021/jo00028a011
日期:1992.1
Rhodium(II) carboxylate catalyzed C-H insertion to form a cyclopentane is shown to compete effectively with beta-hydride elimination, except when the beta-hydrogen is ternary. Cyclization of diazo ester 27 gives 28, which is converted in three steps to (+/-)-tochuinyl acetate 25. Both the cyclization to form 28 and the alkylation of 28 proceed with remarkable diastereoselectivity.