Highly selective chemoenzymatic synthesis of enantiopure orthogonally protected trans-3-amino-4-hydroxypiperidines

Tetrahedron

Volumn 71, Issue 38, 2015, Pages 6907-6912

  Villar Barro, Ángela ^a   Gotor, Vicente ^a   Brieva, Rosario ^a  

^a UNIVERSITY OF OVIEDO   (Spain)

Author keywords

3 Amino 4 hydroxypiperidines; Biocatalysis; Enzymatic resolution; Heterocyclic amino alcohols; Regioselective epoxide opening

Indexed keywords

1 BENZYL 3 (DIALLYLAMINO) 4 HYDROXYPIPERIDINE; 1 BENZYL 3,4 EPOXYPIPERIDINE; 3 AMINO 4 HYDROXYPIPERIDINE DERIVATIVE; AMINOALCOHOL; EPOXIDE; ESTER DERIVATIVE; HYDROXYL GROUP; LIPASE B; ORGANIC SOLVENT; PIPERIDINE DERIVATIVE; UNCLASSIFIED DRUG; VINYL ACETATE;

ACETYLATION; ACYLATION; ARTICLE; CANDIDA ANTARCTICA; DEBENZYLATION; ENANTIOSELECTIVITY; HYDROLYSIS; PRIORITY JOURNAL; RING OPENING; STEREOCHEMISTRY; SYNTHESIS;

CANDIDA ANTARCTICA;

EID: 84940448731     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2015.07.014     Document Type: Article

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