Biocatalyst mediated regio- and stereo-selective hydroxylation and epoxidation of (Z)-α-santalol
Research output: Contribution to journal › Article › peer-review
Standard Standard
In: Organic and Biomolecular Chemistry, Vol. 12, No. 7, 21.02.2014, p. 1048-51.
Research output: Contribution to journal › Article › peer-review
HarvardHarvard
APA
CBE
MLA
VancouverVancouver
Author
RIS
TY - JOUR
T1 - Biocatalyst mediated regio- and stereo-selective hydroxylation and epoxidation of (Z)-α-santalol
AU - Daramwar, Pankaj P
AU - Srivastava, Prabhakar Lal
AU - Kolet, Swati P
AU - Thulasiram, Hirekodathakallu V
PY - 2014/2/21
Y1 - 2014/2/21
N2 - Biocatalyst mediated regio- and stereo-selective hydroxylation and epoxidation on (Z)-α-santalol were achieved for the first time, using a fungal strain Mucor piriformis. Four novel metabolites were characterized as 10,11-cis-β-epoxy-α-santalol, 5α-hydroxy-(Z)-α-santalol, 10,11-dihydroxy-α-santalol and 5α-hydroxy-10,11-cis-β-epoxy-α-santalol. Using Amano PS lipase from Burkholderia cepacia, α- and β-isomers of 10,11-cis-epoxy-α-santalol were resolved efficiently.
AB - Biocatalyst mediated regio- and stereo-selective hydroxylation and epoxidation on (Z)-α-santalol were achieved for the first time, using a fungal strain Mucor piriformis. Four novel metabolites were characterized as 10,11-cis-β-epoxy-α-santalol, 5α-hydroxy-(Z)-α-santalol, 10,11-dihydroxy-α-santalol and 5α-hydroxy-10,11-cis-β-epoxy-α-santalol. Using Amano PS lipase from Burkholderia cepacia, α- and β-isomers of 10,11-cis-epoxy-α-santalol were resolved efficiently.
KW - Biocatalysis
KW - Burkholderia cepacia/enzymology
KW - Hydroxylation
KW - Lipase/metabolism
KW - Molecular Conformation
KW - Mucor/metabolism
KW - Polycyclic Sesquiterpenes
KW - Sesquiterpenes/metabolism
KW - Stereoisomerism
U2 - 10.1039/c3ob42174k
DO - 10.1039/c3ob42174k
M3 - Article
C2 - 24407157
VL - 12
SP - 1048
EP - 1051
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
SN - 1477-0520
IS - 7
ER -