Author:
Hall Laurance D.,Steiner Paul R.,Miller Diane C.
Abstract
Triphenyltin lithium (1) was reacted separately with 1,2:3,5-di-O-methylene-6-O-tosyl-α-D-glucofuranose (2), with methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside (4), and with methyl 2,3-anhydro-4,6-O-benzylidene-α-D-mannopyranoside (6), to form in each case a sugar-stannane derivative having a stable carbon-tin bond. These products have been studied by 1H and 13C nmr spectroscopy.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
23 articles.
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