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Volumn 3, Issue 1-4, 1997, Pages 65-72

A structure-based rationalization of the enantiopreference of subtilisin toward secondary alcohols and isosteric primary amines

Author keywords

Hydrolase; Enantioselectivity; Lipase; Models; Primary amines; Regioselectivity; Secondary alcohols; Subtilase; Subtilisin

Indexed keywords

ALCOHOLS; AMINES; CRYSTAL STRUCTURE; SYNTHESIS (CHEMICAL); X RAY CRYSTALLOGRAPHY;

EID: 0343196675     PISSN: 13811177     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1381-1177(96)00040-9     Document Type: Article
Times cited : (78)

References (47)
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    • Ref. [15] inadvertantly ommitted a note that subtilisin and lipases favor opposite enantiomers of sulcatol. The rules in Fig. 1 correctly predict the favored enantiomer for both. G. Ottolina, personal communication
    • Ottolina et al. Ref. [15] inadvertantly ommitted a note that subtilisin and lipases favor opposite enantiomers of sulcatol. The rules in Fig. 1 correctly predict the favored enantiomer for both. G. Ottolina, personal communication, 1996.
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