Biocatalytic approach for the synthesis of chiral alcohols for the development of pharmaceutical intermediates and other industrial applications: A review

M Naim, MF Mohammat, PNAM Ariff, MH Uzir - Enzyme and Microbial …, 2024 - Elsevier
Biocatalysis has emerged as a strong tool for the synthesis of active pharmaceutical
ingredients (APIs). In the early twentieth century, whole cell biocatalysis was used to …

Preparation of chiral trans-5-substituted-acenaphthene-1, 2-diols by baker's yeast-mediated reduction of 5-substituted-acenaphthylene-1, 2-diones

L Wang, X Wang, J Cui, W Ren, N Meng, J Wang… - Tetrahedron …, 2010 - Elsevier
A series of trans-5-substituted-acenaphthene-1, 2-diols were obtained in 21–72% yield with
97–100% ee by baker's yeast-mediated reduction of the corresponding acenaphthylene-1, 2 …

Use of Saccharomyces cerevisiae yeasts in the chemoselective bioreduction of (1E, 4E)-1, 5-bis (4-methoxyphenyl)-1, 4-pentadien-3-one in biphasic system

CA Schaefer, VD Silva, BU Stambuk… - Journal of the Brazilian …, 2013 - SciELO Brasil
This work describes the chemoselective bioreduction of (1E, 4E)-1, 5-bis (4-methoxyphenyl)-
1, 4-pentadien-3-one (1) mediated by baker's yeast (BY, Saccharomyces cerevisiae cells) in …

Synthesis of new chiral keto alcohols by baker's yeast

T Yıldız, N Canta, A Yusufoğlu - Tetrahedron: Asymmetry, 2014 - Elsevier
Fourteen chiral α-and β-keto alcohols 2a–2r were synthesized by the asymmetric reduction
of their corresponding diketones 1a–1r via baker's yeast. In addition, ten corresponding …

Synthesis, Antibacterial Activity and DFT Calculation of Co (II) and Ni (II) Schiff Bases Complexes Derived from Acenaphthenequinon and Phenylenediamine

QH Al-Hialy, KS Al-Nama - Egyptian Journal of Chemistry, 2021 - journals.ekb.eg
Tetradentate Schiff base ligands. L1=(2Z)-2, 2 ((4-methyl-1, 2-phenylene) bis
(azoneylidine))) bis (acenaphthylene-1 (2H)-one, L2=(2Z, 2E)-2, 2'-((4-nitro-1, 2-phenylene) …

Asymmetric bioreduction of substituted acenaphthenequinones using plant enzymatic systems: A novel strategy for the preparation of (+)-and (−)-mono …

LP Tong, JN Cui, WM Ren, XY Wang, XH Qian - Chinese Chemical Letters, 2008 - Elsevier
Regio-and enantioselective reduction of substituted acenaphthenequinones were
conducted under mild reaction conditions using plant enzymatic systems. A screening of 15 …

[HTML][HTML] Synthesis, Crystal Structure and Antimicrobial Activity of (E)-ethyl-4-(2-oxoacenaphthylen-1(2H)-ylideneamino) benzoate

YC Chan, ASM Ali, M Khairuddean, B Salleh - 2013 - scirp.org
A Schiff base,(E)-ethyl-4-(2-oxoacenaphthylen-1 (2H)-ylideneamino) benzoate,(E4AB) had
been synthesized in good yield by the acid-catalyzed condensation reaction of …

Synthesis of Environmental Relevant Metabolites

E Lindback, MO Sydnes - Petrogenic Polycyclic Aromatic …, 2017 - benthamdirect.com
Polycyclic aromatic hydrocarbons are metabolized in vivo resulting in the formation a range
of oxidized products metabolites. The metabolites generated are more water soluable and …

Yeast‐Mediated Stereoselective Synthesis

R Csuk - Green Biocatalysis, 2016 - Wiley Online Library
Microbial transformations, including yeast or bacterial or enzymatic biotransformations,
bioconversions, or biodegenerations, have been used since the early days of mankind for …

[引用][C] 应用黑曲霉代谢苊醌的影响因素研究

王兴涌, 赵茂爽, 汤海燕, 沙野, 廖梓均 - 中国矿业大学学报, 2013