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Volumn 13, Issue 28, 2015, Pages 7655-7663
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Ring closing metathesis reactions of α-methylene-β-lactams: application to the synthesis of a simplified phyllostictine analogue with herbicidal activity
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Author keywords
[No Author keywords available]
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Indexed keywords
POSITIVE IONS;
CHLAMYDOMONAS REINHARDTII;
HERBICIDAL ACTIVITY;
LACTAM NITROGEN;
MACROCYCLES;
PHYTOTOXIC ACTIVITY;
RING-CLOSING METATHESIS REACTIONS;
STRUCTURAL ELEMENTS;
SUBSTRATE CONCENTRATIONS;
AMIDES;
CHLAMYDOMONAS REINHARDTII;
13-ETHYL-4-OXA-13-AZABICYCLO(10.2.0)TETRADEC-1-EN-14-ONE;
AZABICYCLO DERIVATIVE;
AZETIDINE DERIVATIVE;
FUSED HETEROCYCLIC RINGS;
HERBICIDE;
PHYLLOSTICTINE A;
CHEMICAL STRUCTURE;
CHEMISTRY;
CHLAMYDOMONAS REINHARDTII;
CYCLIZATION;
DOSE RESPONSE;
DRUG EFFECTS;
GROWTH, DEVELOPMENT AND AGING;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
AZABICYCLO COMPOUNDS;
AZETIDINES;
CHLAMYDOMONAS REINHARDTII;
CYCLIZATION;
DOSE-RESPONSE RELATIONSHIP, DRUG;
HERBICIDES;
HETEROCYCLIC COMPOUNDS, 3-RING;
MOLECULAR STRUCTURE;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 84936869297
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/c5ob00890e Document Type: Article |
Times cited : (15)
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References (33)
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