化学
生物催化
硫分解
区域选择性
脂肪酶
催化作用
有机化学
原子经济
组合化学
酶
反应机理
多酚
原花青素
抗氧化剂
作者
Saima Saima,Aditya G. Lavekar,Santosh Kumar,Sumit K. Rastogi,Arun K. Sinha
标识
DOI:10.1080/00397911.2019.1615098
摘要
In this paper, a biocatalytic route is described wherein PPL, lipase from porcine pancreas, in conjunction with water on reaction with different thiophenols and styrene oxides undergo thiolysis with C-S bond formation without the use of any metal catalysts, oxidants, bases, additives or organic solvents towards formation of β-hydroxysulfides in good to excellent yields with high regioselectivity at room temperature. Furthermore, PPL also facilitates thiophenols to undergo hydrothiolation with styrenes or phenylacetylenes in sole water and thus forming linear thioethers or vinylsulfides respectively via C–S bond formation. In addition to the straightforward and atom-efficient protocol, a gram-scale synthesis of β-hydroxysulfide and recyclability for three consecutive cycles without decrease in efficiency of PPL make our biocatalytic protocol for constructing C–S bond highly valuable from both environmental and economic viewpoints than traditional chemical practices.
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