Thio-Claisen rearrangement used in preparing anti-β-functionalized γ,δ-unsaturated amino acids: Scope and limitations

Journal of Organic Chemistry

Volumn 77, Issue 3, 2012, Pages 1289-1300

  Liu, Zhihua ^a   Mehta, Sukeshi J ^a   Lee, Kwang Soo ^a   Grossman, Bryan ^a   Qu, Hongchang ^a   Gu, Xuyuan ^b   Nichol, Gary S ^a   Hruby, Victor J ^a  

^a University of Arizona   (United States)

^b NEKTAR THERAPEUTICS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BUILDING BLOCKES; DIANIONS; FUNCTIONALIZED; OPTICALLY ACTIVE; PEPTIDE CHEMISTRIES; UNSATURATED AMINO ACIDS;

FUNCTIONAL GROUPS; STEREOCHEMISTRY;

AMINO ACIDS;

AMINO ACID; BROMIDE; IRON; IRON BROMIDE; UNCLASSIFIED DRUG;

ALLYLATION; ARTICLE; CHEMICAL REACTION; CHIRALITY; CLAISEN REARRANGEMENT; CONTROLLED STUDY; STEREOCHEMISTRY;

AMINO ACIDS; BROMIDES; CATALYSIS; MODELS, MOLECULAR; MOLECULAR CONFORMATION; STEREOISOMERISM; SULFUR;

EID: 84863011291     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo201753q     Document Type: Article

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