One-pot synthesis of trisubstituted monomethylated benzene-1,3-diols via a Michael addition-Dieckmann cyclization sequence from methyl (E)3-methoxy-4- methoxycarbonylbut-2-enoate anion and methyl alkynoates and its application to the total synthesis of nidulol

Synthesis

Volumn , Issue 14, 2005, Pages 2293-2296

  Covarrubias Zúñiga, Adrián ^a   San Germán Sánchez, Laura ^a   Maldonado, Luis A ^a   Romero Ortega, Moisés ^b   Ávila Zárraga, José G ^a  

^a UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^b UNIVERSIDAD AUTÓNOMA DEL ESTADO DE MÉXICO   (Mexico)

Author keywords

Alkynoates; Dieckmann cyclization; Michael addition; Resorcinol; Tandem reactions

Indexed keywords

ALCOHOLS; DERIVATIVES; NEGATIVE IONS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

ALKYNOATES; DIECKMANN CYCLIZATION; MICHAEL ADDITION; RESORCINOL; TANDEM REACTIONS;

BENZENE;

5 HYDROXY 7 METHOXY 6 METHYLPHTHALIDE; PHTHALIDE DERIVATIVE; RESORCINOL; UNCLASSIFIED DRUG;

ARTICLE; CYCLIZATION; DIECKMANN REACTION; MICHAEL ADDITION; SYNTHESIS;

EID: 24944458538     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-872082     Document Type: Article

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