| Literature DB >> 26337252 |
Zeshan Yousuf1, Andrew K Richards, Andrew N Dwyer, Bruno Linclau, David C Harrowven.
Abstract
A four-step, three-stage synthesis of the API ropinirole hydrochloride has been developed from a commercially available naphthalene derivative. The new route has half the step-count and twice the overall yield of the current manufacturing process. Key features of the synthesis are a regioselective Birch reduction and an ozonolysis with concomitant ring closure to induce the required ring contraction.Entities:
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Year: 2015 PMID: 26337252 DOI: 10.1039/c5ob01739d
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876