Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Nalivela Kumara Swamy"'
Autor:
Bay, Sarah, Englert, Alexandra, Nalivela, Kumara Swamy, Hashmi, A. Stephen K., Larsen, Mie Højer
Publikováno v:
In Journal of Organometallic Chemistry 15 October 2015 795:58-62
Autor:
Nalivela, Kumara Swamy1, Rudolph, Matthias1, Baeissa, Elham S.2, Alhogbi, Basma G.2, Mkhalid, Ibraheem A. I.2, Hashmi, A. Stephen K.1,2 hashmi@hashmi.de
Publikováno v:
Advanced Synthesis & Catalysis. 6/5/2018, Vol. 360 Issue 11, p2183-2190. 8p.
Akademický článek
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Publikováno v:
Tetrahedron Letters. 54:1169-1173
Propargyl ethers and amines are effectively depropargylated to the parent alcohols or amines via a C−O/C−N bond cleavage catalyzed by 10% Pd/C in water. This simple, facile, and inexpensive methodology could be utilized for the selective removal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::492ff8041627542cd7010d1db726fabb
https://doi.org/10.1016/j.tetlet.2012.12.093
https://doi.org/10.1016/j.tetlet.2012.12.093
Autor:
Stephen G. Pyne, Nalivela Kumara Swamy
Publikováno v:
Synthetic Communications. 41:2435-2445
The synthesis of two new trihydroxylated pyrrolidines, in a highly diastereoselective manner, has been developed using the Meyer–Schuster rearrangement as a key step.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c2e85b7bb8b3f693e0a9bc6ade4c1fd
https://doi.org/10.1080/00397911.2010.503003
https://doi.org/10.1080/00397911.2010.503003
Publikováno v:
The Journal of Organic Chemistry. 75:3412-3419
The CuX (X = I, Br, Cl, CN)-mediated cyclization-halogenation and cyclization-cyanation reactions of beta-hydroxyalkynes and o-alkynylphenol and -aniline derivatives give rise to 3-halo- and 3-cyanofuro[3,2-b]pyrroles, 3-iodo-, 3-bromo-, and 3-cyanob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18eb6d7add5311e9b1c84ea47cc241ed
https://doi.org/10.1021/jo1005119
https://doi.org/10.1021/jo1005119
Autor:
Jasmine C, Jury, Nalivela Kumara, Swamy, Arife, Yazici, Ian R, Morgan, Anthony C, Willis, Stephen G, Pyne
Publikováno v:
The Journal of Organic Chemistry. 74:5523-5527
Furo[3,2-b]pyrroles and furo[3,2-b]pyridines can be conveniently prepared in good yields from the cycloisomerization reactions of cis-4-hydroxy-5-alkynylpyrrolidinones and cis-5-hydroxy-6-alkynylpiperidinones, respectively, using Ag(I), Pd(II)/Cu(I),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e99c18cbd877b7359885e55c9ba90768
https://doi.org/10.1021/jo9007942
https://doi.org/10.1021/jo9007942
Autor:
Nalivela Kumara Swamy, Khagga Mukkanti, Manojit Pal, J. Moses Babu, G. Dhananjaya, Rabin Bera, P. Rajender Kumar
Publikováno v:
Tetrahedron. 63:13018-13023
The first Pd/C-mediated Sonogashira coupling of β-chloroacroleins with terminal alkynes is described here. Pd/C–CuI–PPh3 was found to be an efficient catalyst system for this coupling reaction. Using this economic and general process a variety o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52d71b23f19f56af9e84dba940306994
https://doi.org/10.1016/j.tet.2007.10.013
https://doi.org/10.1016/j.tet.2007.10.013
Akademický článek
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Autor:
Manojit Pal, R. Vasu Dev, Bukkapattanam R. Sreekanth, J. Moses Babu, Pazhanimuthu Annamalai, Venkateswara Rao Batchu, Sirisilla Raju, Nalivela Kumara Swamy, Khagga Mukkanti, Krishnamurthi Vyas, P. Rajender Kumar
Publikováno v:
Tetrahedron. 62:9554-9570
We herein report a highly convenient protocol for rapid construction of α-pyrone fused with thiophene. This includes one-pot and regioselective synthesis of 4,5-disubstituted and 5-substituted thieno[2,3- c ]pyran-7-ones, 6,7-disubstituted and 6-sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c85c2290578fe561c33395aa77b9b51
https://doi.org/10.1016/j.tet.2006.07.095
https://doi.org/10.1016/j.tet.2006.07.095