BEMP-promoted C(4)-alkylation of 4-alkyloxazol-5(4 H)-ones: A rapid and efficient route to α,α-dialkyl-α-amino acids

Synlett

Volumn 24, Issue 6, 2013, Pages 701-704

  Lee, Yeon Ju ^a   Seo, Jeyoung ^b   Kim, Dong Guk ^c   Park, Hyeung Geun ^b   Jeong, Byeong Seon ^c  

^a Korea Research Institute of Ships and Ocean Engineering   (South Korea)

^b Seoul National University   (South Korea)

^c Yeungnam University   (South Korea)

Author keywords

, dialkyl amino acid; BEMP; C(4) alkylation; chemoselectivity; oxazol 5(4 H) one; protecting group

Indexed keywords

4 ALKYLOXAZOL 5(4H)ONE DERIVATIVE; ALPHA,ALPHA DIALKYL ALPHA AMINO ACID DERIVATIVE; AMINO ACID DERIVATIVE; OXAZOLE DERIVATIVE; OXAZOLONE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROLYSIS; NUCLEOPHILICITY; STEREOSPECIFICITY;

EID: 84874608430     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0032-1317801     Document Type: Article

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