Access to optically active 2,2′-dihydroxy-6,6′-dimethoxy-1, 1′-biphenyl by a simple biocatalytic procedure

Tetrahedron Asymmetry

Volumn 14, Issue 21, 2003, Pages 3267-3270

  Sanfilippo, Claudia ^a   Nicolosi, Giovanni ^a   Delogu, Giovanna ^a   Fabbri, Davide ^a   Dettori, Maria Antonietta ^a  

^a CNR   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

2,2' DIHYDROXY 6,6' DIMETHOXY 1,1' BIPHENYL; ALCOHOL; BACTERIAL ENZYME; BIPHENYL DERIVATIVE; TERT BUTYL METHYL ETHER; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

ACETYLATION; ARTICLE; BACTERIAL STRAIN; BIOCATALYST; BURKHOLDERIA CEPACIA; CATALYSIS; COMPARATIVE STUDY; ISOMER; OPTICAL ROTATION; PRIORITY JOURNAL; STEREOSPECIFICITY;

EID: 0142165183     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetasy.2003.08.002     Document Type: Article

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40. 3) δ 20.43, 55.99, 56.29, 103.17, 109.13, 109.16, 109.23, 115.07, 115.21, 129.76, 130.01, 150.73, 154.61, 158.00, 158.64, 169.66.
41. The enzyme activity reported by Amano for lipase PS-C and for PS-D is 30U/mg and 8U/mg, respectively.
42. In the same esterification conditions PSL-C, PSL-D and PSL-Celite transformed 2,2′-dihydroxy-1,1′-biphenyl in the corresponding diacetyl derivative; as well as the alcoholysis reactions on 2,2′-diacetoxy-1,1′-biphenyl were successful.