Synthesis of arylglycine and mandelic acid derivatives through carboxylations of α-amido and α-acetoxy stannanes with carbon dioxide

Journal of Organic Chemistry

Volumn 77, Issue 5, 2012, Pages 2159-2168

  Mita, Tsuyoshi ^a   Sugawara, Masumi ^a   Hasegawa, Hiroyuki ^a   Sato, Yoshihiro ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACID DERIVATIVES; INVERSION OF CONFIGURATION; MANDELIC ACID;

CARBOXYLATION; CARBOXYLIC ACIDS; TIN;

CARBON DIOXIDE;

ALPHA ACETOXY STANNANE DERIVATIVE; ALPHA AMIDO STANNANE DERIVATIVE; CARBON DIOXIDE; GLYCINE; MANDELIC ACID DERIVATIVE; ORGANOTIN COMPOUND; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CARBOXYLATION; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CHIRALITY; ENANTIOSELECTIVITY; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

CARBON DIOXIDE; GLYCINE; MANDELIC ACIDS; MOLECULAR STRUCTURE; STEREOISOMERISM; TIN COMPOUNDS;

EID: 84857854773     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo202597p     Document Type: Article

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