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Stereochemistry at C-3 of evernitrose: A fallacy in the determination of stereochemistry at quaternary centres using nuclear magnetic resonance spectroscopy. X-Ray crystal structure of methyl 3-acetamido-2,3,6-trideoxy-3-c, 4-O-dimethyl-L-xylo-hexopyranoside

Publication ,  Journal Article
Ganguly, AK; Sarre, OZ; McPhail, AT; Onan, KD
Published in: Journal of the Chemical Society Chemical Communications
December 1, 1977

Single crystal X-ray analysis of the title compound (8) is reported which establishes the stereochemistry at C-3 of evernitrose.

Duke Scholars

Published In

Journal of the Chemical Society Chemical Communications

DOI

ISSN

0022-4936

Publication Date

December 1, 1977

Issue

9

Start / End Page

313 / 314
 

Citation

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Ganguly, A. K., Sarre, O. Z., McPhail, A. T., & Onan, K. D. (1977). Stereochemistry at C-3 of evernitrose: A fallacy in the determination of stereochemistry at quaternary centres using nuclear magnetic resonance spectroscopy. X-Ray crystal structure of methyl 3-acetamido-2,3,6-trideoxy-3-c, 4-O-dimethyl-L-xylo-hexopyranoside. Journal of the Chemical Society Chemical Communications, (9), 313–314. https://doi.org/10.1039/C39770000313
Ganguly, A. K., O. Z. Sarre, A. T. McPhail, and K. D. Onan. “Stereochemistry at C-3 of evernitrose: A fallacy in the determination of stereochemistry at quaternary centres using nuclear magnetic resonance spectroscopy. X-Ray crystal structure of methyl 3-acetamido-2,3,6-trideoxy-3-c, 4-O-dimethyl-L-xylo-hexopyranoside.” Journal of the Chemical Society Chemical Communications, no. 9 (December 1, 1977): 313–14. https://doi.org/10.1039/C39770000313.

Published In

Journal of the Chemical Society Chemical Communications

DOI

ISSN

0022-4936

Publication Date

December 1, 1977

Issue

9

Start / End Page

313 / 314