α-vinyl β-lactams: Convenient elaboration of the thienamycin side chain Y

Ajay K. Bose; Bimai K. Banik; Sarder N. Newaz; Magbar S. Manbas

doi:10.1055/s-1993-22643

α-vinyl β-lactams: Convenient elaboration of the thienamycin side chain Y

Ajay K. Bose, Bimai K. Banik, Sarder N. Newaz, Magbar S. Manbas

Producción científica: Contribución a una revista › Artículo › revisión exhaustiva

14 Citas (Scopus)

Resumen

β-lactams with the ttienamycin side chain were synthesized from α-vinyl β-lactams via oxymercuration-demercuration reaction as well as through their epoxidation, regioselective epoxide ring cleavage and radical-induced debromination. The stereochemistty of these β-lactams was established by physico-chemicat methods.

Idioma original	Inglés
Páginas (desde-hasta)	897-899
Número de páginas	3
Publicación	Synlett
Volumen	1993
N.º	12
DOI	https://doi.org/10.1055/s-1993-22643
Estado	Publicada - dic. 1993
Publicado de forma externa	Sí

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abstract = "β-lactams with the ttienamycin side chain were synthesized from α-vinyl β-lactams via oxymercuration-demercuration reaction as well as through their epoxidation, regioselective epoxide ring cleavage and radical-induced debromination. The stereochemistty of these β-lactams was established by physico-chemicat methods.",

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AU - Banik, Bimai K.

AU - Newaz, Sarder N.

AU - Manbas, Magbar S.

PY - 1993/12

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AB - β-lactams with the ttienamycin side chain were synthesized from α-vinyl β-lactams via oxymercuration-demercuration reaction as well as through their epoxidation, regioselective epoxide ring cleavage and radical-induced debromination. The stereochemistty of these β-lactams was established by physico-chemicat methods.

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DO - 10.1055/s-1993-22643

M3 - Artículo

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SP - 897

EP - 899

JO - Synlett

JF - Synlett

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α-vinyl β-lactams: Convenient elaboration of the thienamycin side chain Y

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