A ring-closing metathesis-mediated route to novel enantiopure conformationally restricted cyclic amino acids

Chemical Communications

Volumn , Issue 8, 2000, Pages 699-700

  Tjen, Kim C M F ^a   Kinderman, Sape S ^a   Schoemaker, Hans E ^b   Hiemstra, Henk ^a   Rutjes, Floris P J T ^a,c  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

^b DSM RESEARCH   (Netherlands)

^c RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; PIPECOLIC ACID DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CONFORMATION; ENANTIOMER; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 0034696879     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b001253j     Document Type: Article

References (21)

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16. A similar mild reacton was previously observed in our lab upon oxypalladation of benzyl propadienyl ether. The remarkable difference in reactivity with methyl propadienyl ether is not yet understood. R. Doodeman, unpublished work.
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