Ganesan A - Search Results

1

Solid-phase total synthesis of kahalalide A and related analogues.

Bourel-Bonnet L, Rao KV, Hamann MT, Ganesan A. Bourel-Bonnet L, et al. Among authors: ganesan a. J Med Chem. 2005 Mar 10;48(5):1330-5. doi: 10.1021/jm049841x. J Med Chem. 2005. PMID: 15743176 Free PMC article.

2

Synthesis and evaluation of tryprostatin B and demethoxyfumitremorgin C analogues.

Wang H, Usui T, Osada H, Ganesan A. Wang H, et al. Among authors: ganesan a. J Med Chem. 2000 Apr 20;43(8):1577-85. doi: 10.1021/jm9905662. J Med Chem. 2000. PMID: 10780915

3

Solid-phase synthesis of tetrahydro-beta-carbolinehydantoins via the N-acyliminium Pictet-Spengler reaction and cyclative cleavage.

Bonnet D, Ganesan A. Bonnet D, et al. Among authors: ganesan a. J Comb Chem. 2002 Nov-Dec;4(6):546-8. doi: 10.1021/cc020026h. J Comb Chem. 2002. PMID: 12425597 No abstract available.

4

Modular three-component solid-phase synthesis of unsymmetrical guanidines via resin capture of carbodiimides.

Boguszewski PA, Rahman SS, Ganesan A. Boguszewski PA, et al. Among authors: ganesan a. J Comb Chem. 2004 Jan-Feb;6(1):32-4. doi: 10.1021/cc034036+. J Comb Chem. 2004. PMID: 14714980 No abstract available.

5

Cyclative cleavage strategies for the solid-phase synthesis of heterocycles and natural products.

Ganesan A. Ganesan A. Methods Enzymol. 2003;369:415-34. doi: 10.1016/S0076-6879(03)69022-1. Methods Enzymol. 2003. PMID: 14722966 No abstract available.

6

Total synthesis of spiruchostatin A, a potent histone deacetylase inhibitor.

Yurek-George A, Habens F, Brimmell M, Packham G, Ganesan A. Yurek-George A, et al. Among authors: ganesan a. J Am Chem Soc. 2004 Feb 4;126(4):1030-1. doi: 10.1021/ja039258q. J Am Chem Soc. 2004. PMID: 14746465

7

Solid-phase synthesis in the twenty-first century.

Ganesan A. Ganesan A. Mini Rev Med Chem. 2006 Jan;6(1):3-10. doi: 10.2174/138955706775197866. Mini Rev Med Chem. 2006. PMID: 16457628 Review.

8

Total synthesis of azumamide A and azumamide E, evaluation as histone deacetylase inhibitors, and design of a more potent analogue.

Wen S, Carey KL, Nakao Y, Fusetani N, Packham G, Ganesan A. Wen S, et al. Among authors: ganesan a. Org Lett. 2007 Mar 15;9(6):1105-8. doi: 10.1021/ol070046y. Epub 2007 Feb 21. Org Lett. 2007. PMID: 17311393

9

The first biologically active synthetic analogues of FK228, the depsipeptide histone deacetylase inhibitor.

Yurek-George A, Cecil AR, Mo AH, Wen S, Rogers H, Habens F, Maeda S, Yoshida M, Packham G, Ganesan A. Yurek-George A, et al. Among authors: ganesan a. J Med Chem. 2007 Nov 15;50(23):5720-6. doi: 10.1021/jm0703800. Epub 2007 Oct 24. J Med Chem. 2007. PMID: 17958342

10

Macrolactamization versus macrolactonization: total synthesis of FK228, the depsipeptide histone deacetylase inhibitor.

Wen S, Packham G, Ganesan A. Wen S, et al. Among authors: ganesan a. J Org Chem. 2008 Dec 5;73(23):9353-61. doi: 10.1021/jo801866z. J Org Chem. 2008. PMID: 18991384

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