N-Arylmethyl-7-azabicyclo[2.2.1]heptane derivatives: synthesis and reaction mechanisms

Tetrahedron

Volumn 65, Issue 45, 2009, Pages 9224-9232

  Gómez, Elena ^a   Marco Contelles, José ^a   Soriano, Elena ^a   Jimeno, María L ^b  

^a INSTITUTO DE QUÍMICA ORGÁNICA GENERAL   (Spain)

^b CSIC Centro de Quimica Organica Lora Tamayo CENQUIOR   (Spain)

Author keywords

Bromination; Epibatidine analogues; Heterocyclization; N (Arylmethyl)cyclohex 3 enamines; N Arylmethyl 7 azabicyclo 2.2.1 heptanes; Reaction mechanisms

Indexed keywords

7 BENZYL EXO 2 BROMO AZABICYCLO[2.2.1]HEPTANE; BENZYL(CYCLOHEX 3 ENYL)CARBAMATE; ENAMINE; EPIBATIDINE; EXO 2 BROMO 7 (6 CHLOROPYRIDIN 3 YL)METHYL]7 AZABICYCLO[2.2.1]HEPTANE; HEPTANE DERIVATIVE; N (METHYL)CYCLOHEX 3 ENAMINE DERIVATIVE; N BENZYL 3,4 DIBROMOCYCLOHEXANAMINE; N METHYL 7 AZABICYCLO[2.2.1]HEPTANE DERIVATIVE; NICOTINE; TERT BUTYL (6 CHLOROPYRIDIN 3 YL)METHYL(CYCLOHEX 3 ENYL)CARBAMATE; UNCLASSIFIED DRUG;

ARTICLE; BROMINATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; DEPROTECTION REACTION; HYDROLYSIS; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 70349774387     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.09.013     Document Type: Article

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