Preparation of N-protected allylic amines and α-methylene-β- amino acids from vinylalumination/Baylis-Hillman products via tandem S N2′ substitution-Overman rearrangement

Tetrahedron Letters

Volumn 46, Issue 12, 2005, Pages 2121-2124

  Ramachandran, P Veeraraghavan ^a   Burghardt, Thomas E ^a   Reddy, M Venkat Ram ^a,b  

^a PURDUE UNIVERSITY   (United States)

^b UNIVERSITY OF MINNESOTA DULUTH   (United States)

Author keywords

Allylic alcohols; Allylic amines; Baylis Hillman reaction; SN2 reaction; Vinylalumination; Amino acids

Indexed keywords

ACETIC ACID DERIVATIVE; ALCOHOL DERIVATIVE; ALLYL COMPOUND; AMINE; AMINO ACID DERIVATIVE; ESTER; HYDROXYL GROUP; TRICHLOROACETIMIDIC ACID;

ARTICLE; CHEMICAL REACTION; REDUCTION;

EID: 14644412405     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.01.110     Document Type: Article

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