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WJPR Citation
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| All | Since 2020 | |
| Citation | 8502 | 4519 |
| h-index | 30 | 23 |
| i10-index | 227 | 96 |
BIOCATALYTIC REDUCTION OF IMIDAZOL-2-ONES AND PYRIMIDIN-2-ONES MEDIATED BY LYCOPERSICUM ESCULENTUM L (TOMATO)
Dr. Kandarpa Phukan*
Abstract The ripen fruit of Lycopersicum esculentum L (tomato) has been successfully used for enantioselective reduction of Imidazol-2-ones and Pyrimidin-2-ones to the corresponding nitrogenous heterocyclic alcohols. Significantly without using any chemical reducing agents aqueous suspension of ripen tomato fruits alone results in almost complete reduction of a set of five and six membered heterocyclic ketones within 24-35 hrs at room temperature giving corresponding heterocyclic S-alcohols in excellent chemical yields and enantiomeric excess. The present work reveals that chemical transformations using direct plant cells as biocatalysts have now become an attractive and alternative eco-friendly route for synthesis of a variety of commercially significant compounds. Keywords: Biocatalytic reduction, imidazol-2-ones, pyrimidin-2-ones, Lycopersicum esculentum L. [Full Text Article] [Download Certificate] |
