Highly enantioselective synthesis of designed chiral acyclonucleosides and acyclonucleotides by organocatalytic aza-Michael addition

Chemistry - A European Journal

Volumn 17, Issue 15, 2011, Pages 4095-4098

  Guo, Hai Ming ^a   Yuan, Teng Fei ^a   Niu, Hong Ying ^b   Liu, Jin Ying ^a   Mao, Run Ze ^a   Li, De Yang ^a   Qu, Gui Rong ^a  

^a HENAN NORMAL UNIVERSITY   (China)

^b HENAN INSTITUTE OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

acyclonucleosides; acyclonucleotides; aza Michael addition; chirality; organocatalysis

Indexed keywords

ACYCLONUCLEOSIDES; ACYCLONUCLEOTIDES; AZA-MICHAEL ADDITION; ENANTIOSELECTIVE SYNTHESIS; ORGANOCATALYSIS; ORGANOCATALYTIC; PURINE BASIS; UNSATURATED ALDEHYDES;

ALDEHYDES; CATALYSIS; CHIRALITY; ENANTIOMERS; RATE CONSTANTS; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

ADDITION REACTIONS;

HETEROCYCLIC COMPOUND; NUCLEOSIDE; NUCLEOTIDE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

AZA COMPOUNDS; CATALYSIS; MOLECULAR STRUCTURE; NUCLEOSIDES; NUCLEOTIDES; STEREOISOMERISM;

EID: 79953169154     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201100435     Document Type: Article

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