Reaction between N-isocyaniminotriphenylphosphorane, aldimines, Meldrum's acid and water: Diastereoselective synthesis of 3,4-disubstituted N-aminopyrrolidine-2,5-diones

Synlett

Volumn , Issue 5, 2011, Pages 619-622

  Adib, Mehdi ^a   Ansari, Samira ^a   Bijanzadeh, Hamid Reza ^b  

^a UNIVERSITY OF TEHRAN   (Iran)

^b TARBIAT MODARES UNIVERSITY   (Iran)

Author keywords

3,4 disubstituted N aminopyrrolidine 2,5 diones; aldimines; diastereoselective synthesis; Meldrum's acid; multicomponent reactions; N isocyaniminotriphenylphosphorane

Indexed keywords

ALDIMINE DERIVATIVE; N AMINOPYRROLIDINE 2,5 DIONE DERIVATIVE; N ISOCYANIMINOTRIPHENYLPHOSPHORANE; PHOSPHORANE DERIVATIVE; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BIOSYNTHESIS; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; ENVIRONMENTAL TEMPERATURE; HYDROLYSIS; ISOMERIZATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 79952439764     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1259696     Document Type: Article

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