Tetrahedron letters

Use of an iodonium ylide in the synthesis of p-nitrobenzyl (6R, 7S) 3-hydroxy-8-oxo-7-phenoxyacetamino-1-azabicyclo [4.2. 0] octa-2-ene-2-carboxylate

RK Vaid, TE Hopkins

Index: Vaid, Radhe K.; Hopkins, Thomas E. Tetrahedron Letters, 1997 ,  vol. 38,  # 40  p. 6981 - 6984

Full Text: HTML

Citation Number: 8

Abstract

p-Nitrobenzyl (6R, 7S)-3-hydroxy-8-oxo-7-phenoxyacetamido-1-azabicyclo [4.2. 0] octa-2- ene-2-carboxyate (6) was synthesized utilizing rhodium (II)-or acid-catalyzed cyclization of iodonium ylide (5). The iodonium ylide (5) was easily prepared from the corresponding β- keto ester (4) and [(diacetoxy) iodo] benzene in good yield.

Related Articles:

An enantioselective synthesis of loracarbef (LY163892/KT3777)

[Bodurow, C. C.; Boyer, B. D.; Brennan, J.; Bunnell, C. A.; Burks, J. E.; et al. Tetrahedron Letters, 1989 ,  vol. 30,  # 18  p. 2321 - 2324]

An enantioselective synthesis of loracarbef (LY163892/KT3777)

[Bodurow, C. C.; Boyer, B. D.; Brennan, J.; Bunnell, C. A.; Burks, J. E.; et al. Tetrahedron Letters, 1989 ,  vol. 30,  # 18  p. 2321 - 2324]

An enantioselective synthesis of loracarbef (LY163892/KT3777)

[Bodurow, C. C.; Boyer, B. D.; Brennan, J.; Bunnell, C. A.; Burks, J. E.; et al. Tetrahedron Letters, 1989 ,  vol. 30,  # 18  p. 2321 - 2324]

More Articles...