Synthesis of Cytidine, Uridine, and Adenosine 5′-(2,6-Diamino-2,6-dideoxy-α-D-glucopyranosyl diphosphates)(Neosamine C-CDP, -UDP, and -ADP)
Three potential biosynthetic intermediates for aminocyclitol antibiotics, neosamine C-CDP, -UDP, and -ADP, have been synthesized from D-glucosamine by chemical means. 2,6-Diamino-2,6-dideoxy-α-D-glucopyranosyl phosphate, derived from the corresponding glycosyl bromide, was condensed with three nucle...
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Published in | Bulletin of the Chemical Society of Japan Vol. 55; no. 12; pp. 3840 - 3846 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Tokyo
The Chemical Society of Japan
01.12.1982
Chemical Society of Japan |
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Abstract | Three potential biosynthetic intermediates for aminocyclitol antibiotics, neosamine C-CDP, -UDP, and -ADP, have been synthesized from D-glucosamine by chemical means. 2,6-Diamino-2,6-dideoxy-α-D-glucopyranosyl phosphate, derived from the corresponding glycosyl bromide, was condensed with three nucleosides (CMP, UMP and AMP) by a known procedure. The configurations of the neosamine C nucleoside diphosphates have been confirmed by 13C NMR spectra. |
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AbstractList | Abstract
Three potential biosynthetic intermediates for aminocyclitol antibiotics, neosamine C-CDP, -UDP, and -ADP, have been synthesized from d-glucosamine by chemical means. 2,6-Diamino-2,6-dideoxy-α-d-glucopyranosyl phosphate, derived from the corresponding glycosyl bromide, was condensed with three nucleosides (CMP, UMP and AMP) by a known procedure. The configurations of the neosamine C nucleoside diphosphates have been confirmed by 13C NMR spectra. Three potential biosynthetic intermediates for aminocyclitol antibiotics, neosamine C-CDP, -UDP, and -ADP, have been synthesized from D-glucosamine by chemical means. 2,6-Diamino-2,6-dideoxy-α-D-glucopyranosyl phosphate, derived from the corresponding glycosyl bromide, was condensed with three nucleosides (CMP, UMP and AMP) by a known procedure. The configurations of the neosamine C nucleoside diphosphates have been confirmed by 13C NMR spectra. |
Author | Rinehart, Kenneth L Suami, Tetsuo Tadano, Kin-ichi Tsuchiya, Tohru |
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Cites_doi | 10.1002/hlca.19580410607 10.1073/pnas.65.1.19 10.1016/S0008-6215(00)85143-5 10.1016/S0065-2318(08)60219-X 10.1021/ja01601a040 10.1246/bcsj.49.2585 10.1016/S0065-2318(08)60385-6 10.1021/ja01464a035 10.1016/0076-6879(66)08019-4 |
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References | 13)
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Snippet | Three potential biosynthetic intermediates for aminocyclitol antibiotics, neosamine C-CDP, -UDP, and -ADP, have been synthesized from D-glucosamine by chemical... Abstract Three potential biosynthetic intermediates for aminocyclitol antibiotics, neosamine C-CDP, -UDP, and -ADP, have been synthesized from d-glucosamine by... |
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Title | Synthesis of Cytidine, Uridine, and Adenosine 5′-(2,6-Diamino-2,6-dideoxy-α-D-glucopyranosyl diphosphates)(Neosamine C-CDP, -UDP, and -ADP) |
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