Candida antarctica lipase A and Pseudomonas stutzeri lipase as a pair of stereocomplementary enzymes for the resolution of 1,2-diarylethanols and 1,2-diarylethanamines
摘要:
Candida antarctica lipase A (CALA) and Pseudomonas stutzeri lipase (PSL) displayed opposite enantioselectivities in the acylation of 1,2-diphenylethanol and 1,2-diphenylethanamine. CALA was (S)-selective while PSL was (R)-selective. In addition, fourteen different 1,2-diarylethanols were tested as the substrates of CALA. It was found that most of them were accepted by CALA with high enantioselectivity. The DKR of five representative substrates by the combination of CALA and a ruthenium-based racemization catalyst provided good yields (82-91%) and acceptable enantiopurities (87-94% ee). (C) 2012 Elsevier Ltd. All rights reserved.
Candida antarctica lipase A and Pseudomonas stutzeri lipase as a pair of stereocomplementary enzymes for the resolution of 1,2-diarylethanols and 1,2-diarylethanamines
作者:Sol Kim、Yoon Kyung Choi、Jieun Hong、Jaiwook Park、Mahn-Joo Kim
DOI:10.1016/j.tetlet.2012.11.147
日期:2013.3
Candida antarctica lipase A (CALA) and Pseudomonas stutzeri lipase (PSL) displayed opposite enantioselectivities in the acylation of 1,2-diphenylethanol and 1,2-diphenylethanamine. CALA was (S)-selective while PSL was (R)-selective. In addition, fourteen different 1,2-diarylethanols were tested as the substrates of CALA. It was found that most of them were accepted by CALA with high enantioselectivity. The DKR of five representative substrates by the combination of CALA and a ruthenium-based racemization catalyst provided good yields (82-91%) and acceptable enantiopurities (87-94% ee). (C) 2012 Elsevier Ltd. All rights reserved.
β‐Arylation of Racemic Secondary Benzylic Alcohols to Access Enantioenriched β‐Arylated Alcohols
作者:Wang Miao、Jinyu Zhang、Yanyan Yang、Weijun Tang、Dong Xue、Jianliang Xiao、Huaming Sun、Chao Wang
DOI:10.1002/anie.202306015
日期:2023.7.24
catalyst, the first example of β-arylation of secondary alcohols with aryl bromides has been developed via borrowing hydrogen catalysis enabled by an MPV type hydrogen transfer process. In addition, the enantioconvergent version of the reaction has also been realized under the catalysis of Pd and Ru, allowing for the transformation of racemic secondary alcohols into enantioenriched chiral alcohols with good