Jun, SJ Moon, MS Lee, SH Cheong, CS Kim, KS 2024-01-21T04:38:06Z 2024-01-21T04:38:06Z 2021-09-03 2005-07-25 0040-4039 https://pubs.kist.re.kr/handle/201004/136281 Methyl arabinofuranoside 1 was fully acetylated to methyl 2,3,5-tri-O-acetyl-D-arabinofuranoside 2 and it was regio-selectively deacetylated using enzymes. Rhizopus oryzae esterase gave methyl 3,5-di-O-acetyl-D-arabinofuranoside 3, regioselectively. This protected 3 was deoxygenized to 3,5-di-O-acetyl-D-2-deoxyarabinofuranoside 7 using hypophosphorous acid. (c) 2005 Elsevier Ltd. All rights reserved. English PERGAMON-ELSEVIER SCIENCE LTD LIPASE DEOXYGENATION HYDROLYSIS ANALOGS Selective monodeacetylation of methyl 2,3,5-tri-O-acetyl-D-arabinofuranoside using biocatalyst Article 10.1016/j.tetlet.2005.05.120 1 TETRAHEDRON LETTERS, v.46, no.30, pp.5063 - 5065 TETRAHEDRON LETTERS 46 30 5063 5065 scie scopus 000230362300030 2-s2.0-20544432003 Chemistry, Organic Chemistry Article LIPASE DEOXYGENATION HYDROLYSIS ANALOGS arabinose 2-deoxyarabinofuranoside enzyme resolution