TY - JOUR
T1 - Advancements in biocatalysis
T2 - A comprehensive review of applications in organic synthesis
AU - Nayak, Vasavi
AU - D, Deepika
AU - Jude Martis, Glanish
AU - Gaonkar, Santosh L.
N1 - Publisher Copyright:
© 2025 Taylor & Francis Group, LLC.
PY - 2025
Y1 - 2025
N2 - Biocatalysis is an essential tool in the green synthesis of compounds. These catalysts exhibit regioselectivity and stereoselectivity toward specific products, enabling nontoxic and eco-friendly synthetic routes with high-yield biotransformation and enantioselectivity, resulting in enantiopure products. Moreover, the E-factor, which measures the efficiency of a process by calculating the ratio of waste generated to the product formed, is significantly lower in biocatalytic organic synthesis than in traditional methods. The reusability of biocatalysts allows for economically advantageous designs, enabling the reproducibility of products with better yields and energy efficiency in the synthetic route. In this context, enzymes and their modified counterparts have been emphasized as biocatalysts for the biotransformation and asymmetric bio-reduction of various ketones, aldehydes, esters, alcohols, and other substrates.
AB - Biocatalysis is an essential tool in the green synthesis of compounds. These catalysts exhibit regioselectivity and stereoselectivity toward specific products, enabling nontoxic and eco-friendly synthetic routes with high-yield biotransformation and enantioselectivity, resulting in enantiopure products. Moreover, the E-factor, which measures the efficiency of a process by calculating the ratio of waste generated to the product formed, is significantly lower in biocatalytic organic synthesis than in traditional methods. The reusability of biocatalysts allows for economically advantageous designs, enabling the reproducibility of products with better yields and energy efficiency in the synthetic route. In this context, enzymes and their modified counterparts have been emphasized as biocatalysts for the biotransformation and asymmetric bio-reduction of various ketones, aldehydes, esters, alcohols, and other substrates.
UR - https://www.scopus.com/pages/publications/85214653961
UR - https://www.scopus.com/inward/citedby.url?scp=85214653961&partnerID=8YFLogxK
U2 - 10.1080/00397911.2024.2449258
DO - 10.1080/00397911.2024.2449258
M3 - Review article
AN - SCOPUS:85214653961
SN - 0039-7911
JO - Synthetic Communications
JF - Synthetic Communications
ER -