Enantiopure synthesis of all four stereoisomers of carbapenam-3-carboxylic acid methyl ester.
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Mechanism of the C5 Stereoinversion Reaction in the Biosynthesis of Carbapenem AntibioticsBiosynthesis of carbapenem antibiotics: new carbapenam substrates for carbapenem synthase (CarC).Strain-promoted retro-Dieckmann-type condensation on [2.2.2]- and [2.2.1]bicyclic systems: a fragmentation reaction for the preparation of functionalized heterocycles and carbocycles.Three-component synthesis of polysubstituted homoproline analogs.
P2860
Enantiopure synthesis of all four stereoisomers of carbapenam-3-carboxylic acid methyl ester.
description
2003 nî lūn-bûn
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2003年の論文
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name
Enantiopure synthesis of all f ...... -carboxylic acid methyl ester.
@en
Enantiopure synthesis of all f ...... -carboxylic acid methyl ester.
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type
label
Enantiopure synthesis of all f ...... -carboxylic acid methyl ester.
@en
Enantiopure synthesis of all f ...... -carboxylic acid methyl ester.
@nl
prefLabel
Enantiopure synthesis of all f ...... -carboxylic acid methyl ester.
@en
Enantiopure synthesis of all f ...... -carboxylic acid methyl ester.
@nl
P356
P1476
Enantiopure synthesis of all f ...... 3-carboxylic acid methyl ester
@en
P2093
Alberto Avenoza
José I Barriobero
P304
P356
10.1021/JO026804+
P407
P577
2003-04-01T00:00:00Z