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Syntheses of α‐Amino Acids by Using CO 2 as a C1 Source
Author(s) -
Mita Tsuyoshi,
Sato Yoshihiro
Publication year - 2019
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.201900379
Subject(s) - amino acid , chemistry , biochemistry
The incorporation of CO 2 into organic compounds is currently one of the most active research topics in organic chemistry, because CO 2 is an abundant, inexpensive, nontoxic, and renewable C1 source. However, CO 2 is also a thermodynamically stable and kinetically inert gaseous compound, and as such, special strategies are required to activate CO 2 and incorporate it into organic compounds. In particular, because the carbon atom adjacent to the nitrogen atom of amine derivatives is positively charged, umpolung carboxylation, which is a difficult chemical process, should be considered for the production of α‐amino acids by using CO 2 . In this Minireview, we summarize recent synthetic methods for α‐amino acids that use CO 2 as a carboxylic acid unit.

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