Journal of the Chemical Society. Chemical communications p. 449 - 450 (1983)
Update date:2022-08-03
Topics:
Sakakibara, Tohru
Nomura, Yutaka
Yoshino, Kohji
Sudoh, Rokuro
Chlorination of 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol in cyclic ethers such as tetrahydrofuran stereoselectively afforded the ω-chloroalkyl β-D-glucopyranoside derivatives, whereas in 1,4-dioxane α-D-glucopyranosyl chlor
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Doi:10.1039/DT9830001143
(1983)Doi:10.1002/lipd.12213
(2020)Doi:10.1515/znb-2005-0910
(2005)Doi:10.1002/ejoc.200500421
(2006)Doi:10.1007/s11418-017-1118-1
(2018)Doi:10.1039/b811031j
(2008)
