Synthesis of HIV-1 Reverse Transcriptase Inhibitor DMP 266
Author:
Affiliation:
1. a The DuPont Merck Pharmaceutical Company, Chemical Process R&D , Deepwater , NJ , 08023-0999 , U.S.A.
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397919708005064
Reference18 articles.
1. L-743, 726 (DMP-266): a novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase
2. Use of an ephedrine alkoxide to mediate enantioselective addition of an acetylide to a prochiral ketone: asymmetric synthesis of the reverse transcriptase inhibitor L-743,726
3. Ortho functionalization of N-(tert-butoxycarbonyl)aniline
4. Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics
5. Sequential directed ortho metalation reactions. A synthesis ofanthramycin.
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