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Volumn , Issue 20, 2010, Pages 3504-3508
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Synthesis of a novel class of β-lactam derivatives of 1-aminophosphonates by staudinger ketene-imine [2+2]-cycloaddition reaction
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Author keywords
lactams; 1 aminophosphonates; 2+2 cycloaddition reaction; imines; ketenes
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Indexed keywords
1-AMINOPHOSPHONATES;
[2 + 2] CYCLOADDITION;
[2+2]-CYCLOADDITION REACTION;
ACID CHLORIDES;
AMINOPHOSPHONATES;
AROMATIC ALDEHYDE;
CYCLOADDITION REACTION;
IMINES;
KETENES;
TERTIARY AMINE;
ACIDS;
ALDEHYDES;
AMIDES;
CHLORINE COMPOUNDS;
CYCLOADDITION;
SYNTHESIS (CHEMICAL);
1 [(DIETHOXYPHOSPHORYL)PHENYLMETHYL] 2 OXO 4 PHENYLAZETIDI 3 YL ACETATE;
1 AMINOPHOSPHONIC ACID DERIVATIVE;
[(3 METHOXY 2 OXO 4 PHENYLAZETIDIN 1 YL)PHENYLMETHYL]PHOSPHONIC ACID DIETHYL ETHER;
[(3 PHENOXY 2 OXO 4 PHENYLAZETIDIN 1 YL)PHENYLMETHYL]PHOSPHONIC ACID DIETHYL ETHER;
[(4 FLUOROPHENYL) [2 (4 FLUOROPHENYL) 3 METHOXY 4 OXO AZETIDIN 1 YL]METHYL]PHOSPHONIC ACID DIETHYL ETHER;
[(4 METHOXYPHENYL) [2 (4 METHOXYPHENYL) 3 METHOXY 4 OXOAZETIDIN 1 YL]METHYL]PHOSPHONIC ACID DIETHYL ETHER;
[(4 METHOXYPHENYL) [2 (4 METHOXYPHENYL) 3 PHENOXY 4 OXOAZETIDIN 1 YL]METHYL]PHOSPHONIC ACID DIETHYL ETHER;
BETA LACTAM DERIVATIVE;
PHOSPHONIC ACID DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL MODIFICATION;
CYCLOADDITION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
REACTION ANALYSIS;
STAUDINGER REACTION;
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EID: 77957790871
PISSN: 00397881
EISSN: 1437210X
Source Type: Journal
DOI: 10.1055/s-0030-1257889 Document Type: Article |
Times cited : (6)
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References (43)
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