NMR measurements and semi-empirical calculations in a first approach to elucidate the mechanism of enantioselective cyanohydrin formation catalysed by cyclo-(S)-Phe-(S)-His

Tetrahedron: Asymmetry

Volumn 3, Issue 3, 1992, Pages 401-414

  Callant, Dominique ^a   Coussens, Betty ^a   Maten, Taco v d ^a   de Vries, Johannes G ^a   de Vries, N Koen ^a  

^a DSM RESEARCH   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CYANIDE;

ARTICLE; ENANTIOMER; INFRARED SPECTROPHOTOMETRY; NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; SYNTHESIS;

EID: 0026563129     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/S0957-4166(00)80284-0     Document Type: Article

References (26)

1. Cyclo-((S)-leucyl-(S)-histidyl). A catalyst for asymmetric addition of hydrogen cyanide to aldehydes.
2. Evaluation of Some Cyclic Dipeptides as Catalysts for the Asymmetric Hydrocyanation of Aldehydes
3. Asymmetric addition of hydrogen cyanide to substituted benzaldehydes catalyzed by a synthetic cyclic peptide, cyclo((S)-phenylalanyl-(S)-histidyl).
4. Essential Factors in Asymmetric Hydrocyanation Catalyzed by Cyclo(-(R)-Phe-(R)-His-)
5. Asymmetric Hydrocyanation of a Range of Aromatic and Aliphatic Aldehydes
6. N.m.r. studies on the conformation of cyclo(-l-Trp-l-His) in solutions
7. Optimization of parameters for semiempirical methods I. Method
8. Conformation of cyclic dipeptides. The crystal and molecular structures of cyclo-D-alanyl-L-alanyl and cyclo-L-alanyl-L-alanyl (3,6-dimethylpiperazine-2,5-dione)
9. Miscibility of polymer blends investigated by1H spin diffusion and13C NMR detection