Tetrahedron p. 2045 - 2060 (1999)
Update date:2022-09-26
Topics:
Danieli, Bruno
Peri, Francesco
Roda, Gabriella
Carrea, Giacomo
Riva, Sergio
Subtilisin-catalyzed esterification of several enatiomeric benzyl and naphthyl glycopyranosides has been investigated. The D-sugar derivatives were all good substrates and subtilisin regioselectivity was similar with all the compounds tested, the 3-OH being acylated predominantly. On the other hand, most of the L-glycopyranosides were transformed during longer reaction times with a lower regioselectivity, the 2-OH being preferentially but not exclusively acylated.
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Doi:10.1248/cpb.47.226
(1999)Doi:10.1039/a809033e
(1999)Doi:10.1002/zaac.201100040
(2011)Doi:10.1016/j.molstruc.2010.11.037
(2011)Doi:10.1016/j.cclet.2017.10.015
(2018)Doi:10.1016/S0040-4039(99)00215-4
(1999)
