Improved preparation of β-hydroxy-α-amino acids: direct formation of sulfates by sulfuryl chloride
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference48 articles.
1. A short enantioselective synthesis of N-Boc-α-amino acids from epoxy alcohols
2. A Catalytic Asymmetric Synthesis of Cyclohexylnorstatine
3. A Straightforward, Highly Stereoselective Synthesis of Protected Isostatine Derivatives
4. A Catalytic Asymmetric Synthesis of N-Boc-β-Methylphenylalanines
5. Synthesis of N-Boc-β-Aryl Alanines and of N-Boc-β-Methyl-β-aryl Alanines by Regioselective Ring-Opening of Enantiomerically Pure N-Boc-Aziridines
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1. Discovery and Engineering of the l-Threonine Aldolase from Neptunomonas marine for the Efficient Synthesis of β-Hydroxy-α-amino Acids via C–C Formation;ACS Catalysis;2023-05-12
2. Discovery and Engineering of the l-Threonine Aldolase fromNeptunomonas Marinefor Efficient Synthesis of β-Hydroxy-α-Amino Acids via C–C Formation;2023-04-09
3. T211K substitution in Pseudomonas putida phenylserine aldolase improves catalytic efficiency towards l-threo-4-nitrophenylserine with reversed stereoselectivity;Biochemical Engineering Journal;2022-11
4. An L-threonine aldolase for asymmetric synthesis of β-hydroxy-α-amino acids;Chemical Engineering Science;2020-11
5. Engineering of l-threonine aldolase for the preparation of 4-(methylsulfonyl)phenylserine, an important intermediate for the synthesis of florfenicol and thiamphenicol;Enzyme and Microbial Technology;2020-06
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