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KETALS OF L-RHAMNOHEPTONOLACTONES - POTENTIAL MIMICS OF L-RHAMNOSE

Abstract:
Isopropylidene and cyclohexylidene ketals of γ- and δ-heptonolactones derived from Kiliani ascensions of protected L-rhamnose may constitute suitable intermediates for the preparation of mimics of L-rhamnose. The X-ray crystal structure of 7-deoxy-3,4-O-isopropylidene-L-glycero-L-galacto-heptono-1,5-lactone provides an example of a δ-lactone in a boat conformation with a substituent in a flagpole position. The size of ring in the lactones is completely consistent with Hudson's classical lactone rotation rule of 1910. © 1994.
Publication status:
Published

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Publisher copy:
10.1016/S0957-4166(00)80399-7

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Journal:
TETRAHEDRON-ASYMMETRY More from this journal
Volume:
5
Issue:
12
Pages:
2523-2534
Publication date:
1994-12-01
DOI:
EISSN:
1362-511X
ISSN:
0957-4166


Language:
English
Pubs id:
pubs:44628
UUID:
uuid:2c16375e-fe8e-4e9b-b4b8-04d1c9dbe9fc
Local pid:
pubs:44628
Source identifiers:
44628
Deposit date:
2012-12-19

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