Generation of allyl Grignard reagents via titanocene-catalyzed activation of allyl halides
作者:Lauren M. Fleury、Brandon L. Ashfeld
DOI:10.1016/j.tetlet.2010.02.144
日期:2010.5
A protocol for the generation of allylGrignardreagents via the catalytic activation of allyl halides is described herein. Subsequent nucleophilic addition to carbonyl derivatives provided the desired homo allylic alcohols in excellent yields (84–99%). Evidence suggests that titanocene dichloride catalyzes the formation of an allylGrignard species which reacts solely with the carbonyl electrophile
Ti/Pd Bimetallic Systems for the Efficient Allylation of Carbonyl Compounds and Homocoupling Reactions
作者:Alba Millán、Araceli G. Campaña、Btissam Bazdi、Delia Miguel、Luis Álvarez de Cienfuegos、Antonio M. Echavarren、Juan M. Cuerva
DOI:10.1002/chem.201003315
日期:2011.3.28
The allylation, crotylation and prenylation of aldehydes and ketones with stable and easily handled allylic carbonates is promoted by a Ti/Pd catalytic system. This Ti/Pd bimetallic system is especially convenient for the allylation of ketones, which are infrequent substrates in other related protocols, and can be carried out intramolecularly to yield five‐ and six‐membered cyclic products with good
Ti / Pd催化体系可促进醛和酮与稳定且易于处理的烯丙基碳酸酯的烯丙基化,丁酰化和烯丙基化。这种Ti / Pd双金属体系特别适合于酮的烯丙基化,酮是其他相关规程中不常见的底物,并且可以在分子内进行生产,从而产生具有良好立体选择性的五元和六元环状产物。此外,Ti / Pd介导的还原反应和Würtz型二聚反应可以很容易地从碳酸烯丙酯和羧酸酯中进行。
Selective allylation of carbonyl compounds in aqueous media
作者:Cathy Einhorn、Jean-Louis Luche
DOI:10.1016/0022-328x(87)85005-2
日期:1987.3
The use of aqueous neutral media leads to excellent yields of homoallylic alcohols from reaction sof allyl halides with carbonyl compounds in the presence of tin or zinc. The stereochemicalcourse and range of application of this reaction have been investigated.
Indium(I) iodide was found to mediate in the Barbier allylation and in the Reformatsky reaction of aldehydes and ketones to give homoallylic alcohols and β-hydroxy esters, respectively, presumably via allylindium(III) diiodide.
Synthesis and reactivity of benzylic and allylic samarium compounds
作者:C. Bied、J. Collin、H.B. Kagan
DOI:10.1016/s0040-4020(01)88468-4
日期:1992.1
Benzyl and allyl samarium species are prepared by reaction of benzylic or allylicchlorides with SmCp2. They present a wide scope of reactivity towards aldehydes, ketones and acid chlorides.