Please use this identifier to cite or link to this item: http://hdl.handle.net/11717/7685
Title: 1,3:4,6-Di-O-benzylidene-D-mannitol as a source for novel chiral intermediates through regioselective reductive cleavage
Authors: Aravind, A.
Baskaran, S.
Keywords: benzylidene derivative
mannitol
chirality
degradation
quantum yield
reaction analysis
reduction
stereochemistry
synthesis
Issue Date: 2005
Citation: Tetrahedron Letters, 46(5), 743-745
Abstract: Synthetically useful chiral intermediates have been synthesized starting from 1,3:4,6-di-O-benzylidene-D-mannitol by regioselective reductive cleavage using BF 3?Et 2O and Et 3SiH in high yields. ? 2004 Elsevier Ltd. All rights reserved.
URI: http://dx.doi.org/10.1016/j.tetlet.2004.12.036
http://hdl.handle.net/11717/7685
ISSN: 404039
Appears in Collections:Articles

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