Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Satyanarayana, Tummanapalli"'
Autor:
Satyanarayana Tummanapalli, Kali Charan Gulipalli, Srinivas Endoori, Srinu Bodige, Anil Kumar Pommidi, Srinivas Medaboina, Swathi Rejinthala, Suresh Choppadandi, Ravi Boya, Ashok Kanuka, Muralikrishna Valluri
Publikováno v:
Tetrahedron Letters. 104:154022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63e9354a58f3c6ea932b2f6f4db3f548
https://doi.org/10.1016/j.tetlet.2022.154022
https://doi.org/10.1016/j.tetlet.2022.154022
Autor:
Satyanarayana Tummanapalli, Srinu Bodige, Kali Charan Gulipalli, Srinivas Endoori, Srinivas Medaboina, Kalyani Mallidi
Publikováno v:
Tetrahedron Letters. 97:153781
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::deecff919fd60f008f2bddd134d70018
https://doi.org/10.1016/j.tetlet.2022.153781
https://doi.org/10.1016/j.tetlet.2022.153781
Publikováno v:
In Tetrahedron 2007 63(28):6415-6422
Autor:
Satyanarayana Tummanapalli, Dhanunjaya Naidu Vangapandu, Parthasarathy Muthuraman, Sanjeeva Kambampati, Gnanakalai Shanmugavel
Publikováno v:
Tetrahedron Letters. 58:3125-3131
A domino fashioned allylic rearrangement, intramolecular decarboxylative coupling, propargyl-allene rearrangement and diradical 1,3-dien-5-yne cycloaromatization of aryl propiolates of the Baylis-Hillman alcohols in the presence of catalytic Pd(PPh3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64c8bb1eaf39da55609bbd8b14d07a67
https://doi.org/10.1016/j.tetlet.2017.06.079
https://doi.org/10.1016/j.tetlet.2017.06.079
Autor:
Kali Charan Gulipalli, Anil Kumar Pommidi, Shiva Kumar Punna, Satyanarayana Tummanapalli, Divya Vemula, Srinivas Endoori, Srinu Bodige
Publikováno v:
Tetrahedron Letters. 73:153118
Recently new sulfur moieties such as sulfonimidamides are emerging as indispensable bioisosters in medicinal chemistry and agrochemistry programs due to their important biological and physiological properties. But, most available synthetic protocols
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f143ff2f3376eedf37f34f1f5b91f502
https://doi.org/10.1016/j.tetlet.2021.153118
https://doi.org/10.1016/j.tetlet.2021.153118
Autor:
Gnanakalai Shanmugavel, Parthasarathy Muthuraman, Satyanarayana Tummanapalli, Kee Wei Lee, Sanjeeva Kambampati, Dhanunjaya Naidu Vangapandu
Publikováno v:
RSC Advances. 5:49392-49399
Pd-catalyzed decarboxylative allylic coupling of acetates of Baylis–Hillman alcohols with alkynyl carboxylic acids leading to the formation of an important class of 1,5-diarylpent-1-en-4-ynes in a highly regio- and stereoselective manner has been d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c8803b0bee6acd091dbb50353fa3c9f
https://doi.org/10.1039/c5ra06168g
https://doi.org/10.1039/c5ra06168g
Autor:
Satyanarayana, Tummanapalli, Vangapandu, Dhanunjaya Naidu, Muthuraman, Parthasarathy, Nizalapur, Shashidhar
Publikováno v:
In Tetrahedron Letters 8 April 2015 56(15):2008-2013
Autor:
Parthasarathy Muthuraman, Kee Wei Lee, Dhanunjaya Naidu Vangapandu, Gnanakalai Shanmugavel, Satyanarayana Tummanapalli, Sanjeeva Kambampati
Publikováno v:
ChemInform. 46
The title reaction leads to valuable diarylpentenynes in a highly regio- and stereoselective manner via an exclusively SN2′ pathway.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1912ae95242f15c954a5303c68544f9
https://doi.org/10.1002/chin.201541107
https://doi.org/10.1002/chin.201541107
Autor:
Satyanarayana, Tummanapalli, Muthuraman, Parthasarathy, Vangapandu, Dhanunjaya Naidu, Majumder, Supriyo
Publikováno v:
In Tetrahedron Letters 10 December 2014 55(50):6787-6790
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