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Merck
  • Improved catalytic and stereoselective glycosylation with glycosyl N-trichloroacetylcarbamate: application to various 1-hydroxy sugars.

Improved catalytic and stereoselective glycosylation with glycosyl N-trichloroacetylcarbamate: application to various 1-hydroxy sugars.

Carbohydrate research (2010-03-09)
Tatsuya Shirahata, Jun-ichi Matsuo, Satoko Teruya, Nozomu Hirata, Taku Kurimoto, Nanao Akimoto, Toshiaki Sunazuka, Eisuke Kaji, Satoshi Omura
RESUMO

Efficient catalytic and stereoselective glycosylation was achieved by activating a glycosyl N-trichloroacetylcarbamate with a catalytic amount of Lewis acid in the presence of a glycosyl acceptor and 5A molecular sieves. Catalytic one-pot dehydrative glycosylation of a 1-hydroxy carbohydrate was achieved stereoselectively by reaction with trichloroacetyl isocyanate, followed by activation with a catalytic amount of activators.

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Sigma-Aldrich
Trichloroacetyl isocyanate, 96%