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SYNTHETIC STUDIES ON VIRGINIAMYCIN M2: A USEFUL MODEL EXPERIMENT FOR CONSTRUCTION OF THE 1,3-OXAZOLE MOIETY

Author
NAGAO Y; YAMADA S; FUJITA E
KYOTO UNIV., INST. CHEMICAL RES./KYOTO-FU 611/JPN
Source
TETRAHEDRON LETTERS; ISSN 0040-4039; GBR; DA. 1983; VOL. 24; NO 22; PP. 2287-2290; BIBL. 12 REF.
Document type
Article
Language
English
Keyword (fr)
ACYLATION PREPARATION REACTION CHIMIQUE HETEROCYCLE OXYGENE AZOTE CYCLE 5 CHAINONS ANTIBIOTIQUE ADDITION MICHAEL LITHIATION METHYLATION SODIUM HYDRURE!ACT HYDROGENOLYSE BASSE TEMPERATURE REACTION PHOTOCHIMIQUE OXAZOLECARBOXYLIQUE-4 ACIDE(METHYL-2) ESTER T-BUTYLE!ENT OXAZOLECARBOXYLIQUE-4 ACIDE(METHYL-2 TRIMETHYLSILYL-5) ESTER T-BUTYLE PENTANONE-1((METHYL-2 TRIMETHYLSILYL-5 OXAZOLYL-4)-1) OXAZOLECARBOXYLIQUE-4 ACIDE(T-BUTYL-5 METHYL-2) ESTER T-BUTYLE OXAZOLECARBOXYLIQUE-4 ACIDE(BENZENESULFONYLMETHYL-2) ESTER T-BUTYLE OXAZOLECARBOXYLIQUE-4 ACIDE(ALPHA -BENZENESULFONYLPHENACYL-2) ESTER T-BUTYLE!FIN OXAZOLECARBOXYLIQUE-4 ACIDE(OXO-2P NONYL-2) ESTER T-BUTYLE!FIN OXAZOLECARBOXYLIQUE-4 ACIDE(OXO-2P ALKYL-2) ESTER T-BUTYLE!FIN OSTREOGRYCINE G LITHIUM(BUTYL)!ENT LITHIUM(T-BUTYL)!ENT METHANE(IODO)!ENT 18-CROWN-6!ACT THF!SUB OXAZOLECARBOXYLIQUE-4 ACIDE(((T-BUTYL DIMETHYL SILOXY)-4P OXO-2P PENTYL)-2) ESTER T-BUTYLE!FIN CHIMIE ORGANIQUE
Keyword (en)
ACYLATION PREPARATION CHEMICAL REACTION OXYGEN NITROGEN HETEROCYCLE FIVE MEMBERED RING ANTIBIOTIC MICHAEL ADDITION LITHIATION METHYLATION SODIUM HYDRIDES!ACT HYDROGENOLYSIS LOW TEMPERATURE PHOTOCHEMICAL REACTION ORGANIC CHEMISTRY
Keyword (es)
QUIMICA ORGANICA
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL83X0333991

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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