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ω-Transaminase-catalyzed asymmetric synthesis of unnatural amino acids using isopropylamine as an amino donor.
Park, Eul-Soo; Dong, Joo-Young; Shin, Jong-Shik.
Affiliation
  • Park ES; Department of Biotechnology, Yonsei University, 262 Seongsanno, Seodaemun-Gu, 120-749 Seoul, South Korea. enzymo@yonsei.ac.kr.
Org Biomol Chem ; 11(40): 6929-33, 2013 Sep 25.
Article in En | MEDLINE | ID: mdl-23897436
Isopropylamine is an ideal amino donor for reductive amination of carbonyl compounds by ω-transaminase (ω-TA) owing to its cheapness and high volatility of a ketone product. Here we developed asymmetric synthesis of unnatural amino acids via ω-TA-catalyzed amino group transfer between α-keto acids and isopropylamine.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Propylamines / Amino Acids / Transaminases Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2013 Document type: Article Affiliation country: Korea (South) Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Propylamines / Amino Acids / Transaminases Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2013 Document type: Article Affiliation country: Korea (South) Country of publication: United kingdom