Zobrazeno 1 - 5
of 5
pro vyhledávání: '"G. Dattatreya Sarma"'
Autor:
B. Krishna Mohan, G. Dattatreya Sarma, M. Udaya Kiran, Tushar Kanti Chakraborty, S. Uday Kumar, Bharatam Jagadeesh
Publikováno v:
Tetrahedron Letters. 48:6945-6950
Structural analysis of the di- O -caprylated Gaa-containing analog of the receptor binding inhibitors of vasoactive intestinal peptide by various NMR techniques and constrained molecular dynamics (MD) simulation studies established a well-defined β-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a280dbe822447ec8632fb75fc1e7ce12
https://doi.org/10.1016/j.tetlet.2007.07.158
https://doi.org/10.1016/j.tetlet.2007.07.158
Autor:
A. Ganney Parimala, Bhoopendra Tiwari, G. Dattatreya Sarma, Srivari Chandrasekhar, Ch. Narsihmulu
Publikováno v:
Synthesis. 2007:1677-1682
A short and flexible route for the synthesis of 1,2-diisopropyl-3-methyl-(3 S,4 R,5 R)-4,5-dihydroxyhexahydro-1,2,3-pyrid-azinetricarboxylate, from readily available acrolein, is described. This approach involves an asymmetric α-hydrazination, dihyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49347885af4743bed70b421c9ec82997
https://doi.org/10.1055/s-2007-966062
https://doi.org/10.1055/s-2007-966062
Autor:
Nayani Kiranmai, Bharatam Jagadeesh, G. Dattatreya Sarma, Ch. Raji Reddy, Srivari Chandrasekhar, G. S. Kiran Babu
Publikováno v:
Tetrahedron Letters. 48:215-218
The first use of hydroxylamine derivatives as the aminoxy equivalent of nucleophiles in palladium catalyzed addition to Baylis-Hillman acetate adducts is described. The reaction proceeds smoothly to give the substituted allyloxy amines in good yield
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1048b2a88ca9179dfd1486b5050c0de5
https://doi.org/10.1016/j.tetlet.2006.11.061
https://doi.org/10.1016/j.tetlet.2006.11.061
Autor:
Srivari Chandrasekhar, Dolly Vijay, G. Dattatreya Sarma, Bharatam Jagadeesh, B. Saritha, V. Jagadeswar, Ch. Narsihmulu
Publikováno v:
Tetrahedron Letters. 47:2981-2984
Intramolecular hydrogen bonding facilitates nucleophilic addition of sulfones to Baylis-Hillman adducts in a single step to realize the substituted allyl sulfones. The reaction is performed in PEG (400 MW) as solvent, which allows easy solvent recycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3011714e46bef0e019ed5551ab4b44c9
https://doi.org/10.1016/j.tetlet.2006.02.104
https://doi.org/10.1016/j.tetlet.2006.02.104
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