Exploring the synthetic versatility of the lewis acid induced decomposition reaction of α-diazo-β-hydroxy esters. the case of ethyl diazo(3-hydroxy-2-oxo-2,3-dihydro-1 H-indol-3-yl)acetate

Journal of Organic Chemistry

Volumn 76, Issue 18, 2011, Pages 7431-7437

  Gioiello, Antimo ^a   Venturoni, Francesco ^a   Marinozzi, Maura ^a   Natalini, Benedetto ^a   Pellicciari, Roberto ^a  

^a UNIVERSITY OF PERUGIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALDOL-TYPE CONDENSATION; DECOMPOSITION REACTION; ETHYL DIAZOACETATE; EXPERIMENTAL CONDITIONS; HYDROXY ESTERS; LEWIS ACID; MECHANISTIC ASPECTS; MECHANISTIC STUDIES; NUCLEOPHILICITIES; PRODUCT DISTRIBUTIONS;

ESTERIFICATION; VOLATILE FATTY ACIDS;

ESTERS;

ALCOHOL; CATION; DIAZOACETIC ACID ETHYL ESTER; ETHYL DIAZO (3 HYDROXY 2 OXO 2,3 DIHYDRO 1H INDOL 3 YL)ACETATE; INDOLE DERIVATIVE; ISATIN DERIVATIVE; LEWIS ACID; NUCLEOPHILE; SOLVENT; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; COMPLEX FORMATION; DECOMPOSITION; REACTION ANALYSIS; SYNTHESIS;

ACETATES; ESTERS; INDOLES; LEWIS ACIDS;

EID: 80052774743     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo201205u     Document Type: Article

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