Stereoselective tandem Michael-intramolecular cyclization approach to functionalized pyrroloisoindolones

Tetrahedron

Volumn 55, Issue 37, 1999, Pages 11187-11202

  Reyes, Adelfo ^a   Regla, Ignacio ^a   Fragoso, Mabel C ^a   Vallejo, Laura A ^a   Demare, Patricia ^a   Jiménez Vázquez, Hugo A ^b   Ramírez, Yara ^c   Juaristi, Eusebio ^c   Tamariz, Joaquín ^b  

^a UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^b INSTITUTO POLITÉCNICO NACIONAL   (Mexico)

^c DEPARTAMENTO DE FÍSICA   (Mexico)

Author keywords

Cyclization; Michael reactions; N phthaloylalaninate; Pyrroloisoindolones

Indexed keywords

1,2 DICARBOXYETHYL 2,3,5 9B TETRAHYDRO 9B HYDROXY 3 METHYL 5 OXO 1H PYRROLO[2,1 A]ISOINDOLE 3 CARBOXYLIC ACID METHYL ESTER; INDOLE DERIVATIVE; LITHIUM; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; CYCLIZATION; ISOMER; LOW TEMPERATURE; NUCLEAR MAGNETIC RESONANCE; POLYMERIZATION; PRIORITY JOURNAL; STEREOCHEMISTRY; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 0033543472     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00645-6     Document Type: Article

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