The direct utilization of unsaturated sugars in nucleoside syntheses. The synthesis, configuration, and conformation of certain hex-1-enitol-3-yl, hex-2-enopyranosyl-, and hexopyranosylpurines. The preparation of 9-(1,5-anhydro-2,3-dideoxy-D-arabino-hex-1-enitol-3-yl)adenine and 9-(2,3-dideoxy- -D-erythro-hex-2-enopyranosyl)adenine from D-glucal

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Veröffentlicht in:	Journal of organic chemistry 1972-11, Vol.37 (23), p.3695-3702
Hauptverfasser:	Leutzinger, E E, Meguro, T, Townsend, L B
Format:	Artikel
Sprache:	eng
Schlagworte:	Adenine - chemical synthesis Arabinose - chemical synthesis Hexoses Hydrogenation Methods Molecular Conformation Nucleosides - chemical synthesis Purines - chemical synthesis Pyrans - chemical synthesis
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source	ACS Publications; MEDLINE
subjects	Adenine - chemical synthesis Arabinose - chemical synthesis Hexoses Hydrogenation Methods Molecular Conformation Nucleosides - chemical synthesis Purines - chemical synthesis Pyrans - chemical synthesis
title	The direct utilization of unsaturated sugars in nucleoside syntheses. The synthesis, configuration, and conformation of certain hex-1-enitol-3-yl, hex-2-enopyranosyl-, and hexopyranosylpurines. The preparation of 9-(1,5-anhydro-2,3-dideoxy-D-arabino-hex-1-enitol-3-yl)adenine and 9-(2,3-dideoxy- -D-erythro-hex-2-enopyranosyl)adenine from D-glucal
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