Kadow JF - Search Results

1

Development of the Large-Scale Synthesis of Tetrahydropyran Glycine, a Precursor to the HCV NS5A Inhibitor BMS-986097.

Mathur A, Wang B, Smith D, Li J, Pawluczyk J, Sun JH, Wong MK, Krishnananthan S, Wu DR, Sun D, Li P, Yip S, Chen BC, Baran PS, Chen Q, Lopez OD, Yong Z, Bender JA, Nguyen VN, Romine JL, Laurent DRS, Wang G, Kadow JF, Meanwell NA, Belema M, Zhao R. Mathur A, et al. Among authors: kadow jf. J Org Chem. 2017 Oct 6;82(19):10376-10387. doi: 10.1021/acs.joc.7b01852. Epub 2017 Sep 14. J Org Chem. 2017. PMID: 28877441

2

Synthesis and antitumor activity of novel C-7 paclitaxel ethers: discovery of BMS-184476.

Altstadt TJ, Fairchild CR, Golik J, Johnston KA, Kadow JF, Lee FY, Long BH, Rose WC, Vyas DM, Wong H, Wu MJ, Wittman MD. Altstadt TJ, et al. Among authors: kadow jf. J Med Chem. 2001 Dec 20;44(26):4577-83. doi: 10.1021/jm0102607. J Med Chem. 2001. PMID: 11741476

3

A strategy for the synthesis of aryl alpha-ketoamides based upon the acylation of anions derived from cyanomethylamines followed by oxidative cleavage.

Yang Z, Zhang Z, Meanwell NA, Kadow JF, Wang T. Yang Z, et al. Among authors: kadow jf. Org Lett. 2002 Apr 4;4(7):1103-5. doi: 10.1021/ol010297l. Org Lett. 2002. PMID: 11922793

4

A general method for the preparation of 4- and 6-azaindoles.

Zhang Z, Yang Z, Meanwell NA, Kadow JF, Wang T. Zhang Z, et al. Among authors: kadow jf. J Org Chem. 2002 Apr 5;67(7):2345-7. doi: 10.1021/jo0111614. J Org Chem. 2002. PMID: 11925251

5

An effective procedure for the acylation of azaindoles at C-3.

Zhang Z, Yang Z, Wong H, Zhu J, Meanwell NA, Kadow JF, Wang T. Zhang Z, et al. Among authors: kadow jf. J Org Chem. 2002 Aug 23;67(17):6226-7. doi: 10.1021/jo020135i. J Org Chem. 2002. PMID: 12182666

6

Inhibitors of the entry of HIV into host cells.

Meanwell NA, Kadow JF. Meanwell NA, et al. Among authors: kadow jf. Curr Opin Drug Discov Devel. 2003 Jul;6(4):451-61. Curr Opin Drug Discov Devel. 2003. PMID: 12951808 Review.

7

Selective monoacylation of symmetrical diamines via prior complexation with boron.

Zhang Z, Yin Z, Meanwell NA, Kadow JF, Wang T. Zhang Z, et al. Among authors: kadow jf. Org Lett. 2003 Sep 18;5(19):3399-402. doi: 10.1021/ol0300773. Org Lett. 2003. PMID: 12967284

8

Dialkylaminoacetonitrile derivatives as amide synthons. A one-pot preparation of heteroaryl amides via a strategy of sequential SNAr substitution and oxidation.

Zhang Z, Yin Z, Kadow JF, Meanwell NA, Wang T. Zhang Z, et al. Among authors: kadow jf. J Org Chem. 2004 Feb 20;69(4):1360-3. doi: 10.1021/jo030233j. J Org Chem. 2004. PMID: 14961692

9

Acetonitrile derivatives as carbonyl synthons. One-pot preparation of diheteroaryl ketones via a strategy of sequential SNAr substitution and oxidation.

Yin Z, Zhang Z, Kadow JF, Meanwell NA, Wang T. Yin Z, et al. Among authors: kadow jf. J Org Chem. 2004 Feb 20;69(4):1364-7. doi: 10.1021/jo030234b. J Org Chem. 2004. PMID: 14961693

10

Developments in antiviral drug design, discovery and development in 2004.

Meanwell NA, Belema M, Carini DJ, D'Andrea SV, Kadow JF, Krystal M, Naidu BN, Regueiro-Ren A, Scola PM, Sit SY, Walker MA, Wang T, Yeung KS. Meanwell NA, et al. Among authors: kadow jf. Curr Drug Targets Infect Disord. 2005 Dec;5(4):307-400. doi: 10.2174/156800505774912893. Curr Drug Targets Infect Disord. 2005. PMID: 16535860 Review.

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