Development of practical syntheses of potent non-nucleoside reverse transcriptase inhibitors-Reference-Cited by-同舟云学术

Development of practical syntheses of potent non-nucleoside reverse transcriptase inhibitors

Published:2009-06 Issue:26 Volume:65 Page:5013-5023
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Kuethe Jeffrey T.,Zhong Yong-Li,Alam Mahbub,Alorati Anthony D.,Beutner Gregory L.,Cai Dongwei,Fleitz Fred J.,Gibb Andrew D.,Kassim Amude,Linn Kathleen,Mancheno Danny,Marcune Benjamin,Pye Philip J.,Scott Jeremy P.,Tellers David M.,Xiang Bangping,Yasuda Nobuyoshi,Yin Jingjun,Davies Ian W.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Recent Advances in the Development of Next Generation Non-nucleoside Reverse Transcriptase Inhibitors

2. The design and synthesis of diaryl ether second generation HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs) with enhanced potency versus key clinical mutations

3. Discovery of 3-{5-[(6-Amino-1H-pyrazolo[3,4-b]pyridine-3-yl)methoxy]-2-chlorophenoxy}-5-chlorobenzonitrile (MK-4965): A Potent, Orally Bioavailable HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitor with Improved Potency against Key Mutant Viruses

4. Pyrazolo[3,4-b]pyridines: Syntheses, reactions, and nuclear magnetic resonance spectra

5. Optimization of 3-(1H-Indazol-3-ylmethyl)-1,5-benzodiazepines as Potent, Orally Active CCK-A Agonists

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