Literature DB >> 11672382

A Convergent, Scalable Synthesis of HIV Protease Inhibitor PNU-140690.

Kristina S. Fors1, James R. Gage, Richard F. Heier, Robert C. Kelly, William R. Perrault, Nancy Wicnienski.   

Abstract

PNU-140690, an inhibitor of the HIV protease enzyme undergoing clinical evalution as a chemotherapeutic agent for treatment of AIDS, was synthesized by a convergent approach amenable to large-scale preparation in a pilot plant environment. The key step is the aldol addition of nitroaromatic ester (+)-8 to aldehyde 19e. The two stereocenters present in the target molecule were each set independently by resolution of enantiomers. Intermediates along the synthetic routes were chosen to maximize opportunities for isolation and purification by crystallization.

Entities:  

Year:  1998        PMID: 11672382     DOI: 10.1021/jo9809229

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

Review 1.  Catalytic enantioselective olefin metathesis in natural product synthesis. Chiral metal-based complexes that deliver high enantioselectivity and more.

Authors:  Amir H Hoveyda; Steven J Malcolmson; Simon J Meek; Adil R Zhugralin
Journal:  Angew Chem Int Ed Engl       Date:  2010       Impact factor: 15.336

2.  7-Azidomethoxy-coumarins as profluorophores for templated nucleic acid detection.

Authors:  Raphael M Franzini; Eric T Kool
Journal:  Chembiochem       Date:  2008-12-15       Impact factor: 3.164

3.  An expeditious and efficient bromomethylation of thiols: enabling bromomethyl sulfides as useful building blocks.

Authors:  Carolina Silva-Cuevas; Ehecatl Paleo; David F León-Rayo; J Armando Lujan-Montelongo
Journal:  RSC Adv       Date:  2018-07-10       Impact factor: 4.036

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.