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

Research output: Contribution to journal › Article › peer-review

14 Scopus citations

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.

Original language	English
Pages (from-to)	897-899
Number of pages	3
Journal	Synlett
Volume	1993
Issue number	12
DOIs	https://doi.org/10.1055/s-1993-22643
State	Published - Dec 1993
Externally published	Yes

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title = "α-vinyl β-lactams: Convenient elaboration of the thienamycin side chain Y",

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.",

author = "Bose, {Ajay K.} and Banik, {Bimai K.} and Newaz, {Sarder N.} and Manbas, {Magbar S.}",

year = "1993",

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AU - Banik, Bimai K.

AU - Newaz, Sarder N.

AU - Manbas, Magbar S.

PY - 1993/12

Y1 - 1993/12

N2 - 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.

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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VL - 1993

SP - 897

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JO - Synlett

JF - Synlett

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ER -

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

Abstract

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