Chemo- and regioselective 4CR synthesis of oxathiaaza[33.3]propellanes via sequential C-S, C-N and C-O bond formation in a single pot

Synlett

Volumn 23, Issue 17, 2012, Pages 2526-2530

  Rezvanian, Atieh ^a   Alizadeh, Abdolali ^a   Zhu, Long Guan ^b  

^a TARBIAT MODARES UNIVERSITY   (Iran)

^b ZHEJIANG UNIVERSITY   (China)

Author keywords

chemoselectivity; four component reaction (4CR); oxathiaaza 3.3.3 propellanes; regioselectivity

Indexed keywords

8C AMINO 2 (4 CHLOROPHENYLIMINO) 3 ETHYL 8 OXO 2,3 DIHYDRO 8H 8D OXA 1 THIA 3 AZAPENTALENO[3A,6A A]INDEN 8 YL CYANIDE; 8C AMINO 2 (4 CHLOROPHENYLIMINO) 3 ISOBUTYL 8 OXO 2 (4 METHYLPHENYLIMINO) 2,3 DIHYDRO 8H 8D OXA 1 THIA 3 AZAPENTALENO[3A,6A A]INDEN 8 YL CYANIDE; 8C AMINO 2 (4 CHLOROPHENYLIMINO) 8 OXO 3 PROPYL 2,3 DIHYDRO 8H 8D OXA 1 THIA 3 AZAPENTALENO[3A,6A A]INDEN 8 YL CYANIDE; 8C AMINO 2 (4 METHYLPHENYLIMINO) 8 OXO 3 PROPYL 2,3 DIHYDRO 8H 8D OXA 1 THIA 3 AZAPENTALENO[3A,6A A]INDEN 8 YL CYANIDE; 8C AMINO 3 ETHYL 8 OXO 2 (4 METHYLPHENYLIMINO) 2,3 DIHYDRO 8H 8D OXA 1 THIA 3 AZAPENTALENO[3A,6A A]INDEN 8 YL CYANIDE; 8C AMINO 3 ETHYL 8 OXO 2 PHENYLIMINO 2,3 DIHYDRO 8H 8D OXA 1 THIA 3 AZAPENTALENO[3A,6A A]INDEN 8 YL CYANIDE; 8C AMINO 3 ISOBUTYL 8 OXO 2 (4 METHYLPHENYLIMINO) 2,3 DIHYDRO 8H 8D OXA 1 THIA 3 AZAPENTALENO[3A,6A A]INDEN 8 YL CYANIDE; 8C AMINO 3 ISOBUTYL 8 OXO 2 PHENYLIMINO 2,3 DIHYDRO 8H 8D OXA 1 THIA 3 AZAPENTALENO[3A,6A A]INDEN 8 YL CYANIDE; 8C AMINO 3 METHYL 2 (4 METHYLPHENYLIMINO) 8 OXO 2,3 DIHYDRO 8H 8D OXA 1 THIA 3 AZAPENTALENO[3A,6A A]INDEN 8 YL CYANIDE; 8C AMINO 3 METHYL 8 OXO 2 PHENYLIMINO 2,3 DIHYDRO 8H 8D OXA 1 THIA 3 AZAPENTALENO[3A,6A A]INDEN 8 YL CYANIDE; 8C AMINO 8 OXO 2 PHENYLIMINO 3 PROPYL 2,3 DIHYDRO 8H 8D OXA 1 THIA 3 AZAPENTALENO[3A,6A A]INDEN 8 YL CYANIDE; AMINE; MALONONITRILE; NINHYDRIN; OXATHIAAZA[3.3.3]PROPELLANE DERIVATIVE; UNCLASSIFIED DRUG;

ABSORPTION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLOADDITION; DIELS ALDER REACTION; ELECTROPHILICITY; KNOEVENAGEL CONDENSATION; MICHAEL ADDITION; NUCLEOPHILICITY; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS;

EID: 84866678645     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0032-1317181     Document Type: Article

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