Synthesis of methyl 2,3,6-trideoxy-4-C-(2,5-dimethoxybenzyl)-α-L-threo-hex-2-enopyranoside

Article abstract of DOI:10.1080/07328309808002326

Methyl 2,3-O-protected α-L-lyxopyranosid-4-uloses (9 and 19), obtained from L-rhamnose (8), react with 2,5-dimethoxybenzyllithium to afford, with high stereoselectivity, compounds 10a and 20a, respectively. After protection of the 4-OH group, ethers 10b a

Full text of DOI:10.1080/07328309808002326

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Journal of Carbohydrate Chemistry
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Synthesis of Methyl 2,3,6-Trideoxy-4-C-
(2,5-dimethoxybenzyl)-α-l-threo-hex-2-
enopyranoside
Osman Achmatowicz a , Barbara Szechner a & Jan K. Maurin b
a Pharmaceutical Research Institute , 8 Rydygiera Str., 01-793,
Warszawa, Poland
b Institute of Atomic Energy , 05-400, Otwock-Swierk, Poland
Published online: 16 Aug 2006.
To cite this article: Osman Achmatowicz , Barbara Szechner & Jan K. Maurin (1998) Synthesis
of Methyl 2,3,6-Trideoxy-4-C-(2,5-dimethoxybenzyl)-α-l-threo-hex-2-enopyranoside, Journal of
Carbohydrate Chemistry, 17:2, 249-266, DOI: 10.1080/07328309808002326
To link to this article: http://dx.doi.org/10.1080/07328309808002326
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