Zobrazeno 1 - 10
of 55
pro vyhledávání: '"H. Rama Mohan"'
Autor:
Y. Satish Kumar, Ch. Muralikrishna, Satish S. More, M.V. Basaveswara Rao, Thalishetti Krishna, M. V. Madhubabu, Raghunadh Akula, R. Shankar, Y. Chiranjeevi, H. Rama Mohan
Publikováno v:
Tetrahedron: Asymmetry. 28:1803-1807
A convergent approach towards the synthesis of the 2-alkyl-substituted tetrahydroquinoline alkaloid (−)-cuspareine via enantiospecific construction of the (R)-benzyl 2-formyl-3,4-dihydroquinoline-1(2H)-carboxylate. We have achieved an efficient ena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2d16e9ad58897c5fabf4b0c80f763b2
https://doi.org/10.1016/j.tetasy.2017.10.023
https://doi.org/10.1016/j.tetasy.2017.10.023
Publikováno v:
Asian Journal of Chemistry. 29:1853-1858
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1d66cefc1e7f10eb7dbcaf38797f8f4
https://doi.org/10.14233/ajchem.2017.20679
https://doi.org/10.14233/ajchem.2017.20679
Autor:
T.V. Pratap, Sandip R. Khobare, H. Rama Mohan, Vidavalur Siddaiah, Srinivasa Reddy Kallam, Vikas Gajare, Muralikrishna Kommi, Rajender Datrika
Publikováno v:
Tetrahedron: Asymmetry. 27:603-607
A concise total synthesis of ( R )-(−)-phoracantholide I 1 and ( S )-(+)-phoracantholide I 2 has been developed from ( R )-(+)-γ-valerolactone 6 . The key steps in the synthesis of these macrolides involved enzymatic reduction of Levulinic ester 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd72e50877eab36b1df1a31d2e0e2aac
https://doi.org/10.1016/j.tetasy.2016.05.008
https://doi.org/10.1016/j.tetasy.2016.05.008
Autor:
M., Shankar1,2, H., Rama Mohan1, U., Viplava Prasad2, M., Harikrishna1, M. P., Pareswar Rao1, A., Ravindra1
Publikováno v:
Journal of Heterocyclic Chemistry. Jul2014, Vol. 51 Issue 4, p1086-1093. 8p.
Autor:
Nagaraju Rajana, T.V. Pratap, Vidavalur Siddaiah, J. Moses Babu, H. Rama Mohan, Rajender Datrika, Srinivasa Reddy Kallam, Vikas Gajare, Sandip R. Khobare
Publikováno v:
Tetrahedron Letters. 57:1351-1353
Highly stereoselective total syntheses of polyhydroxylated piperidines d -fagomine and 2- epi -fagomine have been developed starting from 3,4,6-tri- O -benzyl- d -glucal which is a derivative of d -Glucose. Key steps in the synthesis of these azasuga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c69273b7aa8efdbb71c9f0788ae45b3a
https://doi.org/10.1016/j.tetlet.2016.02.046
https://doi.org/10.1016/j.tetlet.2016.02.046
Publikováno v:
Journal of Heterocyclic Chemistry. 51:1086-1093
A general synthetic approach has been developed for heterocyclic prostaglandins (PGF2α type) starting from the key intermediate (6). (±) 6 was obtained from (±) -Corey lactone. The key intermediate (±) 6 was, in turn, converted in to several new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76889e9397d64f28f5d18f11a819a8ac
https://doi.org/10.1002/jhet.1622
https://doi.org/10.1002/jhet.1622
Publikováno v:
Asian Journal of Chemistry. 26:7439-7543
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fc288468f5137ca5f18d739261dead6
https://doi.org/10.14233/ajchem.2014.16794
https://doi.org/10.14233/ajchem.2014.16794
Publikováno v:
Asian Journal of Chemistry. 26:1921-1930
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8195b26503c8aa51672955a31eb90fe6
https://doi.org/10.14233/ajchem.2014.15564
https://doi.org/10.14233/ajchem.2014.15564
Autor:
Vidavalur Siddaiah, Muralikrishna Kommi, Vikas Gajare, Sandip R. Khobare, Rajender Datrika, T.V. Pratap, Srinivasa Reddy Kallam, H. Rama Mohan
Publikováno v:
ChemInform. 47
A concise total synthesis of ( R )-(−)-phoracantholide I 1 and ( S )-(+)-phoracantholide I 2 has been developed from ( R )-(+)-γ-valerolactone 6 . The key steps in the synthesis of these macrolides involved enzymatic reduction of Levulinic ester 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebebbed8f9cbf038a1717af4b3d2e271
https://doi.org/10.1002/chin.201647216
https://doi.org/10.1002/chin.201647216
Publikováno v:
Synthetic Communications. 42:1288-1305
A general synthetic approach has been developed for the synthesis of a key intermediate (6) that can be elaborated into several ophthalmic prostaglandins and their derivatives. Using these strategy, we have obtained (±)-bimatoprost (1) and its analo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::496f78d73ba374535a294f915151eac8
https://doi.org/10.1080/00397911.2010.539754
https://doi.org/10.1080/00397911.2010.539754