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Sulfur Ylide Vinylation of Halides and Mesylates
Le Gall,T.,Martel, J. P.,Harnett, J. J.,Shin,Dong-Soo,Flack, J. R.,Mioskowski, C.,Alcaraz, L. 國立昌原大學校 基礎科學硏究所 1994 基礎科學硏究所論文集 Vol.6 No.-
One-carbon homologation of benzylic, allylic, propargylic and primary halides or mesylates with dimethylsulfonium methylide affords terminal olefins in good to excellent yields.
A Novel Synthesis of Homologated Allylic Alcohols Using Dimethylsulphonium Methylide
Le Gall, T.,Harnett, J. J.,Alcaraz, L.,Shin,Dong-Soo,Flack, J. R.,Mioskowski, C.,Martel, J. P. 國立昌原大學校 基礎科學硏究所 1994 基礎科學硏究所論文集 Vol.6 No.-
The reaction of excess dimethylsulphonium methylide with various aliphatic and aromatic ketones leads exclusively to homologated allylic alcohols in good yields.
Mioskowski, C.,Alcaraz, L.,Flack, J. R.,Shin,Dong-Soo,Le Gall, T.,Martel, J. P.,Harnett, J. J. 國立昌原大學校 基礎科學硏究所 1994 基礎科學硏究所論文集 Vol.6 No.-
The reaction of excess of dimethylsulfonium methylide with terminal, allylic, or benzylic epoxides affords good to excellent yields of one carbon homologated allylic alcohols.