EASY SYNTHESIS OF 1-ALLYL-1-DEOXY-β- AND α- d -LYXOFURANOSES
Publication type: Journal Article
Publication date: 2002-05-31
scimago Q3
wos Q2
SJR: 0.369
CiteScore: 2.1
Impact factor: 2.2
ISSN: 07328303, 15322327
Organic Chemistry
Biochemistry
Abstract
2,3;5,6-Di-O-isopropylidene-α-d-mannofuranosyl chloride reacted with allylmagnesium bromide with preferential inversion of the anomeric configuration to furnish a mixture of the 1-allyl-1-deoxy-β- and α-d-mannofuranoses. Separation of β and α derivatives was possible only after conversion to the 1-allyl-1-deoxylyxofuranoses 2 and 3. The β configuration of the predominant product 2 was proved using the NOE method.
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Total citations:
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GOST
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Doboszewski B. EASY SYNTHESIS OF 1-ALLYL-1-DEOXY-β- AND α- d-LYXOFURANOSES // Journal of Carbohydrate Chemistry. 2002. Vol. 21. No. 1-2. pp. 79-88.
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Doboszewski B. EASY SYNTHESIS OF 1-ALLYL-1-DEOXY-β- AND α- d-LYXOFURANOSES // Journal of Carbohydrate Chemistry. 2002. Vol. 21. No. 1-2. pp. 79-88.
Cite this
RIS
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TY - JOUR
DO - 10.1081/car-120003739
UR - https://doi.org/10.1081/car-120003739
TI - EASY SYNTHESIS OF 1-ALLYL-1-DEOXY-β- AND α- d-LYXOFURANOSES
T2 - Journal of Carbohydrate Chemistry
AU - Doboszewski, Bogdan
PY - 2002
DA - 2002/05/31
PB - Taylor & Francis
SP - 79-88
IS - 1-2
VL - 21
SN - 0732-8303
SN - 1532-2327
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2002_Doboszewski,
author = {Bogdan Doboszewski},
title = {EASY SYNTHESIS OF 1-ALLYL-1-DEOXY-β- AND α- d-LYXOFURANOSES},
journal = {Journal of Carbohydrate Chemistry},
year = {2002},
volume = {21},
publisher = {Taylor & Francis},
month = {may},
url = {https://doi.org/10.1081/car-120003739},
number = {1-2},
pages = {79--88},
doi = {10.1081/car-120003739}
}
Cite this
MLA
Copy
Doboszewski, Bogdan. “EASY SYNTHESIS OF 1-ALLYL-1-DEOXY-β- AND α- d-LYXOFURANOSES.” Journal of Carbohydrate Chemistry, vol. 21, no. 1-2, May. 2002, pp. 79-88. https://doi.org/10.1081/car-120003739.