| dc.contributor.author | Mear, Sarah Jane | |
| dc.contributor.author | Lucas, Tobias | |
| dc.contributor.author | Ahlqvist, Grace P | |
| dc.contributor.author | Robey, Juliana MS | |
| dc.contributor.author | Dietz, Jule‐Philipp | |
| dc.contributor.author | Khairnar, Pankaj V | |
| dc.contributor.author | Maity, Sanjay | |
| dc.contributor.author | Williams, Corshai L | |
| dc.contributor.author | Snead, David R | |
| dc.contributor.author | Nelson, Ryan C | |
| dc.contributor.author | Opatz, Till | |
| dc.contributor.author | Jamison, Timothy F | |
| dc.date.accessioned | 2022-10-06T15:13:40Z | |
| dc.date.available | 2022-10-06T15:13:40Z | |
| dc.date.issued | 2022-08-22 | |
| dc.identifier.uri | https://hdl.handle.net/1721.1/145710 | |
| dc.description.abstract | Bedaquiline is a crucial medicine in the global fight against tuberculosis, yet its high price places it out of reach for many patients. Herein, we describe improvements to the key industrial lithiation-addition sequence that enable a higher yielding and therefore more economical synthesis of bedaquiline. Prioritization of mechanistic understanding and multi-lab reproducibility led to optimized reaction conditions that feature an unusual base-salt pairing and afford a doubling of the yield of racemic bedaquiline. We anticipate that implementation of these improvements on manufacturing scale will be facile, thereby substantially increasing the accessibility of this essential medication. | en_US |
| dc.language.iso | en | |
| dc.publisher | Wiley | en_US |
| dc.relation.isversionof | 10.1002/chem.202201311 | en_US |
| dc.rights | Creative Commons Attribution 4.0 International license | en_US |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | en_US |
| dc.source | Wiley | en_US |
| dc.title | Diastereoselectivity is in the Details: Minor Changes Yield Major Improvements to the Synthesis of Bedaquiline** | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Mear, Sarah Jane, Lucas, Tobias, Ahlqvist, Grace P, Robey, Juliana MS, Dietz, Jule‐Philipp et al. 2022. "Diastereoselectivity is in the Details: Minor Changes Yield Major Improvements to the Synthesis of Bedaquiline**." Chemistry – A European Journal, 28 (47). | |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
| dc.relation.journal | Chemistry – A European Journal | en_US |
| dc.eprint.version | Final published version | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dc.date.updated | 2022-10-06T15:06:49Z | |
| dspace.orderedauthors | Mear, SJ; Lucas, T; Ahlqvist, GP; Robey, JMS; Dietz, J; Khairnar, PV; Maity, S; Williams, CL; Snead, DR; Nelson, RC; Opatz, T; Jamison, TF | en_US |
| dspace.date.submission | 2022-10-06T15:06:53Z | |
| mit.journal.volume | 28 | en_US |
| mit.journal.issue | 47 | en_US |
| mit.license | PUBLISHER_CC | |
| mit.metadata.status | Authority Work and Publication Information Needed | en_US |