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Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives

Vadim Borisovich Krylov 1
Vadim Borisovich Krylov
, 
Dmitry Anatol'evich Argunov 1
Dmitry Anatol'evich Argunov
, 
Nikolay Eduardovich Nifantiev 1
Nikolay Eduardovich Nifantiev
10.1016/j.mencom.2014.11.006
Published 2014-10-30
Communication , Volume 24, Issue 6, 336-337
7
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Krylov V. B., Argunov D. A., Nifantiev N. E. Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives // Mendeleev Communications. 2014. Vol. 24. No. 6. pp. 336-337.
GOST all authors (up to 50) Copy
Krylov V. B., Argunov D. A., Nifantiev N. E. Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives // Mendeleev Communications. 2014. Vol. 24. No. 6. pp. 336-337.
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TY - JOUR
DO - 10.1016/j.mencom.2014.11.006
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2014.11.006
TI - Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives
T2 - Mendeleev Communications
AU - Krylov, Vadim Borisovich
AU - Argunov, Dmitry Anatol'evich
AU - Nifantiev, Nikolay Eduardovich
PY - 2014
DA - 2014/10/30
PB - Mendeleev Communications
SP - 336-337
IS - 6
VL - 24
ER -
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@article{2014_Krylov,
author = {Vadim Borisovich Krylov and Dmitry Anatol'evich Argunov and Nikolay Eduardovich Nifantiev},
title = {Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives},
journal = {Mendeleev Communications},
year = {2014},
volume = {24},
publisher = {Mendeleev Communications},
month = {Oct},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2014.11.006},
number = {6},
pages = {336--337},
doi = {10.1016/j.mencom.2014.11.006}
}
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Krylov, Vadim Borisovich, et al. “Preparative synthesis of selectively substituted 1,6-anhydro-α-D-galactofuranose derivatives.” Mendeleev Communications, vol. 24, no. 6, Oct. 2014, pp. 336-337. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2014.11.006.

Abstract

Heating of trisodium salt of allyl 3-O-benzyl-2,5,6-tri-O-sulfonato-β-D-galactofuranoside with pyridinium chloride in dioxane affords 1,6-anhydro-3-O-benzyl-α-D-galactofuranose which was regioselectively acylated to give useful precursors for oligosaccharide synthesis.

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