Mondal D - Search Results

1

Improved Methodology for the Synthesis of a Cathepsin B Cleavable Dipeptide Linker, Widely Used in Antibody-Drug Conjugate Research.

Mondal D, Ford J, Pinney KG. Mondal D, et al. Tetrahedron Lett. 2018 Oct 3;59(40):3594-3599. doi: 10.1016/j.tetlet.2018.08.021. Epub 2018 Aug 14. Tetrahedron Lett. 2018. PMID: 31156276 Free PMC article.

2

Efficient Synthetic Methodology for the Construction of Dihydronaphthalene and Benzosuberene Molecular Frameworks.

Mondal D, Niu H, Pinney KG. Mondal D, et al. Tetrahedron Lett. 2019 Jan 31;60(5):397-401. doi: 10.1016/j.tetlet.2018.12.033. Epub 2018 Dec 16. Tetrahedron Lett. 2019. PMID: 31061544 Free PMC article.

3

Structure Guided Design, Synthesis, and Biological Evaluation of Novel Benzosuberene Analogues as Inhibitors of Tubulin Polymerization.

Niu H, Strecker TE, Gerberich JL, Campbell JW 3rd, Saha D, Mondal D, Hamel E, Chaplin DJ, Mason RP, Trawick ML, Pinney KG. Niu H, et al. Among authors: mondal d. J Med Chem. 2019 Jun 13;62(11):5594-5615. doi: 10.1021/acs.jmedchem.9b00551. Epub 2019 May 24. J Med Chem. 2019. PMID: 31059248 Free PMC article.

4

Bioreductively Activatable Prodrug Conjugates of Combretastatin A-1 and Combretastatin A-4 as Anticancer Agents Targeted toward Tumor-Associated Hypoxia.

Winn BA, Devkota L, Kuch B, MacDonough MT, Strecker TE, Wang Y, Shi Z, Gerberich JL, Mondal D, Ramirez AJ, Hamel E, Chaplin DJ, Davis P, Mason RP, Trawick ML, Pinney KG. Winn BA, et al. Among authors: mondal d. J Nat Prod. 2020 Apr 24;83(4):937-954. doi: 10.1021/acs.jnatprod.9b00773. Epub 2020 Mar 20. J Nat Prod. 2020. PMID: 32196334 Free PMC article.

5

Recent advances in heterolytic nucleofugal leaving groups.

Lepore SD, Mondal D. Lepore SD, et al. Among authors: mondal d. Tetrahedron. 2007 Jun 11;63(24):5103-5122. doi: 10.1016/j.tet.2007.03.049. Tetrahedron. 2007. PMID: 19568330 Free PMC article. No abstract available.

6

Rapid conversion of hindered arylsulfonates to alkyl chlorides with retention of configuration.

Lepore SD, Bhunia AK, Mondal D, Cohn PC, Lefkowitz C. Lepore SD, et al. Among authors: mondal d. J Org Chem. 2006 Apr 14;71(8):3285-6. doi: 10.1021/jo052333q. J Org Chem. 2006. PMID: 16599631 Free PMC article.

7

Stereoretentive halogenations and azidations with titanium(IV) enabled by chelating leaving groups.

Lepore SD, Mondal D, Li SY, Bhunia AK. Lepore SD, et al. Among authors: mondal d. Angew Chem Int Ed Engl. 2008;47(39):7511-4. doi: 10.1002/anie.200802472. Angew Chem Int Ed Engl. 2008. PMID: 18712737 No abstract available.

8

Stereoretentive chlorination of cyclic alcohols catalyzed by titanium(IV) tetrachloride: evidence for a front side attack mechanism.

Mondal D, Li SY, Bellucci L, Laino T, Tafi A, Guccione S, Lepore SD. Mondal D, et al. J Org Chem. 2013 Mar 1;78(5):2118-27. doi: 10.1021/jo3023439. Epub 2013 Jan 23. J Org Chem. 2013. PMID: 23298402 Free PMC article.

9

A Direct and Stereoretentive Synthesis of Amides from Cyclic Alcohols.

Mondal D, Bellucci L, Lepore SD. Mondal D, et al. European J Org Chem. 2011 Dec;2011(35):10.1002/ejoc.201101165. doi: 10.1002/ejoc.201101165. European J Org Chem. 2011. PMID: 24273447 Free PMC article.

10

Nucleophile assisting leaving groups: a strategy for aliphatic 18F-fluorination.

Lu S, Lepore SD, Li SY, Mondal D, Cohn PC, Bhunia AK, Pike VW. Lu S, et al. Among authors: mondal d. J Org Chem. 2009 Aug 7;74(15):5290-6. doi: 10.1021/jo900700j. J Org Chem. 2009. PMID: 19572583 Free PMC article.

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