Mendu Narender


Arbeitsgebiet

Stereoselektive Synthese photolabiler Aminosäuren

Publikationen

1. “A new asymmetric synthetic route to substituted piperidines” M. Somi Reddy, M. Narender and K. Rama Rao, “Tetrahedron”, 2007, 63, 331.

2. “Stereoselective synthesis of simplactone B via prins cyclization” M. Somi Reddy, M. Narender and K. Rama Rao, “Tetrahedron”, 2007, 63, 11011.

3. “Supramolecular synthesis of selenazoles using selenourea in water in the presence of β- cyclodextrin under atmospheric pressure” M. Narender, M. Somi Reddy, V. Pavan Kumar, V. Prakash Reddy, Y. V. D. Nageswar and K. Rama Rao, “J. Org. Chem.2007, 72, 1849.

4. “β-cyclodextrin catalysed mono-sulfonylation of amines and amino acids in water” R. Sridhar, B. Srinivas, V. Pavan Kumar, M. Narender and K. Rama Rao, “Adv. Synth. Catal.2007, 349, 1873-1876.

5. “Friedel-Crafts alkylation of indoles with nitroolefins in the presence of β-cyclodextrin in water under neutral conditions” V. Pavan Kumar, R. Sridhar, B. Srinivas, M. Narender and K. Rama Rao, Can. J. Chem. 2008, 86, 907.

6. “Aqueous phase one-pot synthesis of 2-amino-5-carboxylate thiazoles/selenazoles from β-ketoesters, thiourea/selenourea and NBS under supramolecular catalysis” M. Narender, M. Somi Reddy, V. Pavan Kumar, B. Srinivas, R. Sridhar and K. Rama Rao, “Synthesis2007, 22, 3469.

7. “Highly regioselective C(3) opening of an aromatic 2,3-epoxy alcohol with sodium phenoxides or thiophenoxides (=benzenethiolates) supported by β-cyclodextrin in water” M. Narender, M. Somi Reddy, Y. V. D. Nageswar and K. Rama Rao, “Helv. Chim. Acta.2007, 90, 1107.

8. “β-Cyclodextrin-supported, completely regioselective ring opening of thiaranes with thiophenol in water” M. Somi Reddy, K. Surendra, N. S. Krishnaveni, M. Narender and K. Rama Rao, “Helv. Chim. Acta.” 2007, 90, 337.

9. “Synthesis of thiazoles and aminothiazoles from β-keto tosylates under supramolecular catalysis in the presence of β-cyclodextrin in water” V. Pavan Kumar, M. Narender, R. Sridhar, Y.V.D. Nageswar and K. Rama Rao, “Synth. Commun.2007, 37, 4331.

10. “Supramolecular catalyzed synthesis of 3-indolyl-3-hydroxy oxindoles under neutral conditions in water” V. Pavan Kumar, V. Prakash Reddy, R. Sridhar, B. Srinivas, M. Narender, K. Rama Rao, "J. Org. Chem." 2008, 73, 1646.

11. “N-Boc protection of amines with di-tert-butyldicarbonate in water under neutral conditions in the presence of β-cyclodextrin” M. Somi Reddy, M. Narender, Y. V. D. Nageswar and K. Rama Rao, “Synlett”, 2006, 07, 1110.

12. “Aqueous phase mono-protection of amines and amino acids as N-benzyloxycarbonyl derivatives in the presence of β-cyclodextrin” V. Pavan Kumar, M. Somi Reddy, M. Narender, K. Surendra, Y. V. D. Nageswar and K. Rama Rao, “Tetrahedron Lett.” 2006, 47, 6393.

13. “Highly regioselective thiolysis of oxiranes under supramolecular catalysis involving β- cyclodextrin in water” M. Somi Reddy, B. Srinivas, R. Sridhar, M. Narender, and K. Rama Rao, “J. Mol. Cat. A: Chemical. 2006, 255, 180.

14. “Aqueous phase synthesis of vic-halohydrins from olefins and N-halosuccinimides in the presence of β-cyclodextrin” M. Narender, M. Somi Reddy, Y. V. D. Nageswar and K. Rama Rao, “J. Mol. Cat. A: Chemical.2006, 258, 10.

15. “Facile deprotection of 1,3-oxathiolanes to carbonyl compounds with O-Iodoxy benzoic acid (IBX) in the presence of β-cyclodextrin in water” M. Somi Reddy, M. Narender, A. Mahesh, Y. V. D. Nageswar and K. Rama Rao, “Synth. Commun.2006, 36, 3771.

16. “Deprotection of oximes using iodosobenzene in the presence of β-cyclodextrin in water” M. Narender, M. Somi Reddy, N. S. Krishnaveni, K. Surendra, Y. V. D. Nageswar and K. Rama Rao, “Synth. Commun. 2006, 36, 1463.

17. “Regioselective ring-opening of aziridines with thiophenol in the presence of β-cyclodextrin in water” M. Somi Reddy, M. Narender and K. Rama Rao, “Synlett”, 2005, 03, 0489.

18. “Aqueous phase synthesis of thiazoles and aminothiazoles in the presence of β-cyclodextrin” M. Narender, M. Somi Reddy, R. Sridhar, Y. V. D. Nageswar and K. Rama Rao, “Tetrahedron Lett.2005, 46, 5953.

19. “Regioselective ring-opening of aziridines with potassium thiocyanate in the presence of β-cyclodextrin in water” M. Somi Reddy, M. Narender, Y. V. D. Nageswar and K. Rama Rao, “Tetrahedron Lett.2005, 46, 6437.

20. “Direct synthesis of carbonyl compounds from THP ethers with IBX in the presence of β-cyclodextrin in water” M. Narender, M. Somi Reddy, V. Pavan Kumar, Y. V. D. Nageswar and K. Rama Rao, “Tetrahedron Lett.2005, 46, 1971.

21. “A mild and efficient synthesis of α-tosylamino ketones from aryl aziridines in the presence of β-cyclodextrin and NBS in water” M. Somi Reddy, M. Narender and K. Rama Rao, “Tetrahedron Lett.2005, 46, 1299.

22. “Organic reactions in water: Synthesis of phenacyl esters from phenacyl bromide and potassium salts of aromatic acids in the presence of β-cyclodextrin” M. Narender, M. Somi Reddy, V. Pavan Kumar and K. Rama Rao, “Synth. Commun. 2005, 35, 1681.

23. “A facile β-cyclodextrin-catalyzed oxidative deprotection of tert-butyldimethylsilyl (TBDMS) ethers with NBS in water” M. Somi Reddy, M. Narender, Y. V. D. Nageswar and K. Rama Rao, “Synthesis”, 2005, 05, 0714.

24. “A facile regioselective ring opening of aziridines to haloamines using tetrabutylammonium halides in the presence of β-cyclodextrin in water” M. Narender, K. Surendra, N. Srilakshmi Krishnaveni, M. Somi Reddy and K. Rama Rao, “Tetrahedron Lett.2004, 45, 7995.

25. “A mild and efficient oxidative deprotection of THP ethers with NBS in the presence of β-cyclodextrin in water” M. Narender, M. Somi Reddy and K. Rama Rao, “Synthesis”, 2004, 11, 1741.

26. “Highly efficient regioselective ring opening of aziridines to β-haloamines in the presence of β-cyclodextrin in water” N. Srilakshmi Krishnaveni, K. Surendra, M. Narender, Y.V.D. Nageswar and K. Rama Rao, “Synthesis2004, 04, 0501.

27. “Regeneration of carbonyl compounds by oxidative cleavage of oximes with NBS in the presence of β-cyclodextrin in water” M. Somi Reddy, M. Narender and K. Rama Rao, “Synth. Commun.2004, 34, 3875.

28. “Simple one-pot procedure for the generation of homoallylic alcohols from Barbier-type allylation of gem-diacetates in the presence of β-cyclodextrin in water” M. Somi Reddy, M. Narender, Y. V. D. Nageswar and K. Rama Rao “Synth. Commun.2007, 37, 1983.