trans-3-Aryl-4-nitro-pyrrolidines via 1,3-dipolar cycloaddition of nonstabilized azomethine ylide to ß-nitro styrenes

Tetrahedron

Volumn 51, Issue 24, 1995, Pages 6783-6788

  Nyerges, Miklós ^a   Balázs, László ^a   Kádas, István ^a   Bitter, István ^a   Kövesdi, István ^b   Tőke, László ^a  

^a INSTITUTE OF EXPERIMENTAL MEDICINE   (Hungary)

^b EGIS PHARMACEUTICALS LTD   (Hungary)

Author keywords

[No Author keywords available]

Indexed keywords

NITRO DERIVATIVE; PYRROLIDINE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0029020883     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(95)00311-U     Document Type: Article

References (29)

1. A Short and New Synthesis of Optically Pure (+)-Retronecine
2. A new and efficient strategy for non-stabilized azomethine ylide via photoinduced electron transfer (PET) initiated sequential double desilylation
3. Amino acid approach as a general route to nonstabilized azomethine ylides. Facile generation of parent methaniminium methylide and its 1-mono- and 1,1-disubstituted derivatives.