Highly efficient catalytic asymmetric acylation of meso-1,2-diols with benzoyl chloride in the presence of a chiral diamine combined with Et3N

Tetrahedron Letters

Volumn 39, Issue 21, 1998, Pages 3529-3532

  Oriyama, Takeshi ^a   Imai, Keisuke ^a   Sano, Tomohumi ^a   Hosoya, Takeshi ^a  

^a IBARAKI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; DIAMINE; PROLINE; TRIETHYLAMINE;

ACYLATION; ARTICLE; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0032554989     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00523-1     Document Type: Article

References (25)

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24. A screening of a series of chiral diamines validated the occurrence of face-selection, and (S)-1-methyl-2-[(benzylmethylamino)methyl]pyrrolidine was found to be the chiral diamine of choice.
25. 3)).