Efficient synthesis of optically active herbicide (S)-metolachlor via reductive ring opening of 2-methoxymethylaziridine
Title | Efficient synthesis of optically active herbicide (S)-metolachlor via reductive ring opening of 2-methoxymethylaziridine |
Publication Type | Journal Article |
Year of Publication | 2023 |
Authors | Nalla, V, Mujahid, M, Sasikumar, M, Mujumdar, P, Muthukrishnan, M |
Journal | Arkivoc |
Date Published | JUL |
Type of Article | Article |
ISSN | 1551-7004 |
Keywords | Aziridine, Epoxide, Epoxide ring opening, herbicide synthesis, Metolachlor |
Abstract | An efficient synthesis of a well known chiral herbicide, (S)-metolachlor has been described using 2methoxymethylaziridine ring formation and reductive ring opening as key steps using commercially available (R)-epichlorohydrin. The present protocol delivers the required enantiomer of metolachlor in overall yield of 50.8% and high enantiopurity (>99%). |
DOI | 10.24820/ark.5550190.p011.954 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 0.9 |
Divison category:
Organic Chemistry
Database:
Web of Science (WoS)
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