Journal of the Chemical Society. Chemical communications p. 1993 - 1994 (1995)
Update date:2022-07-30
Topics:
Cipolla, Laura
Lay, Luigi
Nicotra, Francesco
Panza, Luigi
Russo, Giovanni
Reaction of 2,3,5-tri-O-benzyl-D-arabinose with divinylzinc, and subsequent mercuriocyclisation and iodomercuriation stereoselectively affords the α-C-glucopyranosyl iodide 3 with a free hydroxy group at C-2; temporary protection of the free hydroxy group
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