Synthesis of optically pure 4-hydroxymethyl-3-phenoxy-2-azetidinone from D-glucal
Synthesis of optically pure 4-hydroxymethyl-3-phenoxy-2-azetidinone from D-glucal
A convenient approach to enantiomerically pure 4-hydroxymethyl- 3-phenoxy-2-azetidinone has been carried out using the easily available aldehyde 5 as chiral starting material.
staudinger reaction, beta-lactam, ozonolysis, beta-lactams, chiral auxiliary, asymmetric-synthesis, carbohydrate
857-862
Areces, P.
e88f0d0f-33ff-4e7a-8839-c6237abf795e
Carrasco, E.
2351eaf8-a83e-476f-99fc-a3601ec5949c
Monterde, M.
13e4d0de-54d5-4c57-997b-04a655e1b38d
Light, M.E.
cf57314e-6856-491b-a8d2-2dffc452e161
Plumet, J.
9709c2cf-1cd0-4ba0-b982-a18212bb560f
2007
Areces, P.
e88f0d0f-33ff-4e7a-8839-c6237abf795e
Carrasco, E.
2351eaf8-a83e-476f-99fc-a3601ec5949c
Monterde, M.
13e4d0de-54d5-4c57-997b-04a655e1b38d
Light, M.E.
cf57314e-6856-491b-a8d2-2dffc452e161
Plumet, J.
9709c2cf-1cd0-4ba0-b982-a18212bb560f
Areces, P., Carrasco, E., Monterde, M., Light, M.E. and Plumet, J.
(2007)
Synthesis of optically pure 4-hydroxymethyl-3-phenoxy-2-azetidinone from D-glucal.
Heterocycles, 73 (1), .
Abstract
A convenient approach to enantiomerically pure 4-hydroxymethyl- 3-phenoxy-2-azetidinone has been carried out using the easily available aldehyde 5 as chiral starting material.
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Published date: 2007
Keywords:
staudinger reaction, beta-lactam, ozonolysis, beta-lactams, chiral auxiliary, asymmetric-synthesis, carbohydrate
Identifiers
Local EPrints ID: 54237
URI: http://eprints.soton.ac.uk/id/eprint/54237
ISSN: 1881-0942
PURE UUID: 7d9430e4-d810-4b09-9948-76e30382e711
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Date deposited: 31 Jul 2008
Last modified: 09 Jan 2022 02:59
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Contributors
Author:
P. Areces
Author:
E. Carrasco
Author:
M. Monterde
Author:
J. Plumet
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