Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Sulfoxide-metal exchange

Likewise, the sulfoxide-metal exchange reaction of /3-acetoxy sulfoxides 164 (/3-mesyloxy sulfoxides can also be used), which are prepared from alkenyl aryl sulfoxides 163 and aromatic aldehydes, with a Grignard or alkyllithium reagent at low temperatures gives the allenes 162 in good to excellent yield (Scheme 5.24) [65],... [Pg.205]

The male bean weevil sex attractant has been made by a new method of allene synthesis from aldehydes and alkenyl aryl sulfoxides by sulfoxide-metal exchange as the key reaction. [Pg.317]

H - Metal exchange or Halogen - Metal exchange or Sulfoxide - Metal exchange reaction... [Pg.718]

In 1993, Satoh and coworkers reported the preparation of lithium- and magnesium-aUtylidene carbenoids from 1-chlorovinyl phenyl sulfoxides by sulfoxide-metal exchange reaction at low temperature (Scheme 6). 1-Chlorovinyl phenyl sulfoxide (128) is easily synthesized from the corresponding aldehyde and chloromethyl phenyl sulfoxide in high yield. Sulfoxide 128 was treated with f-BuLi in THF at —78 °C to give the terminal alkyne 131. Obviously, the intermediate of this reaction was the alkylidene carbenoid 129. [Pg.743]

SCHEME 28.10 Mechanistic scenarios for the sulfoxide/metal exchange. [Pg.822]

SCHEME 28.17 Sulfoxide/metal exchange for the generation of arynes. [Pg.826]

The synthesis of 3 was initiated by reaction of wBuLi with the protected cyclopentenone 2 generating the corresponding vinyllithium reagent by halogen-metal exchange. Subsequent condensation with (S)-(-)-menthyl para-toluenesulfinate (13) provides the enantiodefined sulfoxide substituent in 3.5 Since thermal equilibration of chiral sulfoxides at room temperature is slow, the large sulfur atom is a preferred reaction site in synthetic intermediates to introduce chirality into carbon compounds. [Pg.6]

Zirconium tetrachloride is instantly hydrolyzed in water to zirconium oxide dichloride octahydrate [13520-92-8]. Zirconium tetrachloride exchanges chlorine for 0x0 bonds in the reaction with hydroxylic ligands, forming alkoxides from alcohols (see Alkoxides, METAl). Zirconium tetrachloride combines with many Lewis bases such as dimethyl sulfoxide, phosphoms oxychloride and amines including ammonia, ethers, and ketones. The zirconium organometalLic compounds ate all derived from zirconium tetrachloride. [Pg.435]


See other pages where Sulfoxide-metal exchange is mentioned: [Pg.720]    [Pg.720]    [Pg.553]    [Pg.65]    [Pg.813]    [Pg.138]    [Pg.133]    [Pg.134]    [Pg.454]    [Pg.720]    [Pg.720]    [Pg.553]    [Pg.65]    [Pg.813]    [Pg.138]    [Pg.133]    [Pg.134]    [Pg.454]    [Pg.238]    [Pg.718]    [Pg.737]    [Pg.119]    [Pg.143]    [Pg.167]    [Pg.170]    [Pg.197]    [Pg.201]    [Pg.40]    [Pg.188]    [Pg.813]    [Pg.822]    [Pg.822]    [Pg.823]    [Pg.826]    [Pg.110]    [Pg.189]    [Pg.279]    [Pg.212]    [Pg.167]    [Pg.150]    [Pg.345]    [Pg.464]    [Pg.14]    [Pg.24]   
See also in sourсe #XX -- [ Pg.134 ]




SEARCH



Metal sulfoxidation

Sulfoxide-metal exchange reactions

Sulfoxides sulfur-metal exchange

© 2024 chempedia.info