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Corey-Chaykovsky reagent

Dimethyloxosulfonium methylide - known as the Corey-Chaykovsky Reagent - is a valuable alternative to dimethylsulfonium methylide and can be generated from trimethylsulfoxonium iodide. [Pg.80]

The reaction of the Corey-Chaykovsky Reagent with enones is a 1,4-addition that is followed by ring closure to give a cyclopropane ... [Pg.81]

Ng, J. S. Epoxide formation from aldehydes and ketones - a modified method for preparing the Corey-Chaykovsky reagents. Synth. Commun. 1990, 20,1193-1202. [Pg.565]

In addition to the synthesis of heterocycles, the Corey-Chaykovsky reaction bestows an entry to carbocycles as well. The reaction of (trialkylsilyl)vinylketene 89 with substituted ylide 90 led exclusively to rrans-4,5-dimethyl cyclopentenone 91. The substituted ylide 90 here serves as a nucleophilic carbenoid reagent in the formal [4 +1] annulation reaction. [Pg.12]

The most commonly used reagents to effect the addition of a methylene group to an aldehyde or ketone are sulfur ylides such as dimethylsulfonium methylide (1) or dimethyloxosulfonium methylide (2) (Corey-Chaykovsky reaction). This reaction is well reviewed in standard treatises of organic synthesis - and several useful monographs. - This update will concentrate on progress attained from 1975. The reader is also encouraged to consult reviews on the chemistry of the related sulfoximine-derived ylides such as (3). -"... [Pg.820]

Corey and Chaykovsky had discovered that dimethyl sulfoxide is converted to methyl-sulfinyl carbanion upon treatment with sodium hydride114 and that this conjugate base of DMSO reacts with various electrophiles115. This finding has opened up various reactions with a-sulfmyl carbanions derived from sulfoxides, since the sulfinyl function can be removed either by thermolysis or by subjecting the compound to reductive desulfurization. Thus a-sulfmyl carbanions have become versatile synthetically useful reagents. [Pg.606]

Details of the preparation and use of the reagent are provided E. J. Corey, M. Chaykovsky, Journal of the American Chemical Society 1965, 87,1350... [Pg.743]


See other pages where Corey-Chaykovsky reagent is mentioned: [Pg.743]    [Pg.713]    [Pg.743]    [Pg.713]    [Pg.10]    [Pg.872]    [Pg.64]    [Pg.199]    [Pg.102]    [Pg.53]    [Pg.149]    [Pg.1169]    [Pg.1386]    [Pg.158]    [Pg.889]    [Pg.360]    [Pg.65]    [Pg.771]   
See also in sourсe #XX -- [ Pg.174 , Pg.530 , Pg.743 ]

See also in sourсe #XX -- [ Pg.174 , Pg.530 , Pg.743 ]




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