Zobrazeno 1 - 10
of 16
pro vyhledávání: '"M. Rajashekhar Reddy"'
Publikováno v:
SSRN Electronic Journal.
Autor:
G. Ravi Kumar, M. Rajashekhar Reddy, D. Yogananda Chary, Swarnayu Banik, B. Sridhar, B.V. Subba Reddy
Publikováno v:
Tetrahedron Letters. 110:154174
Autor:
M. Rajashekhar Reddy, B. V. Subba Reddy, Boora Ramesh, C. Ravikumar Reddy, Suresh Yarlagadda, B. Sridhar
Publikováno v:
European Journal of Organic Chemistry. 2017:2332-2337
Autor:
M. Rajashekhar Reddy, G. Ravi Kumar, Suresh Yarlagadda, B. Sridhar, J. S. Yadav, C. Ravikumar Reddy, B. V. Subba Reddy
Publikováno v:
RSC Advances. 6:113390-113394
Various aldehydes undergo a smooth cascade cyclization with N-(5-hydroxypent-2-yn-1-yl)-4-methyl-N-phenylbenzenesulfonamide in the presence of 10 mol% Ph3PAuCl/AgSbF6/In(OTf)3 to furnish the corresponding tetrahydro-2H-pyrano[3,4-c]quinoline derivati
Autor:
M. Rajashekhar Reddy, C. Ravikumar Reddy, Suresh Yarlagadda, G. Ravi Kumar, B. Sridhar, J. S. Yadav, B. V. Subba Reddy
Publikováno v:
The Journal of Organic Chemistry. 80:8807-8814
A domino cyclization of 3-((3-(2-aminophenyl)prop-2-ynylamino)methyl)but-3-en-1-ol with aldehydes has been accomplished employing 5 mol % of the Ph3PAuCl/AgSbF6/In(OTf)3 system to afford the corresponding octahydrospiro[pyran-4,4'-pyrido[3,4-b]indole
Autor:
Dayaka Satyanarayana, Bharatam Jagadeesh, B. Sridhar, M. Rajashekhar Reddy, Basi V. Subba Reddy, C. Ravikumar Reddy, Suresh Yarlagadda
Publikováno v:
European Journal of Organic Chemistry. 2015:3076-3085
Cascade cyclization of a 3-[(3-methylbut-2-enylamino)methyl]but-3-en-1-ol derivative with aldehydes in the presence of TMSOTf at 0 °C under mild conditions provides the corresponding spiropyrrolidine scaffolds in good yields. Similar cyclization of
Autor:
B. V. Subba Reddy, Suresh Yarlagadda, J. S. Yadav, C. Ravikumar Reddy, G. Ravi Kumar, M. Rajashekhar Reddy, B. Sridhar
Publikováno v:
ChemInform. 47
A domino cyclization of 3-((3-(2-aminophenyl)prop-2-ynylamino)methyl)but-3-en-1-ol with aldehydes has been accomplished employing 5 mol % of the Ph3PAuCl/AgSbF6/In(OTf)3 system to afford the corresponding octahydrospiro[pyran-4,4′-pyrido[3,4-b]indo
Publikováno v:
ChemInform. 46
The novel strategy is based on an oxidative two-step transformation of hydrazine dicarboxylates with aryl iodides.
Publikováno v:
Organic letters. 17(15)
A wide range of benzo[c]cinnolines are prepared through a sequential C–C and C–N bond formation by means of an oxidative C–H functionalization. The reaction proceeds via the C-arylation of 1-arylhydrazine-1,2-dicarboxylate with aryl iodide usin
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