Zobrazeno 1 - 10
of 30
pro vyhledávání: '"K. Papi Reddy"'
Publikováno v:
Synthetic Communications. 43:26-33
An efficient, simple, and practical method has been developed for the deprotection of prenyl, geranyl, and phytyl ethers and esters of aromatic and aliphatic compounds using borontrifluoride–etherate (BF3 · OEt2) at room temperature in good to exc
Autor:
Tadigoppula Narender, null Dharamsheela, Jayanta Sarkar, K. Papi Reddy, G. Madhur, Satinath Sarkar, Raj Kamal Tripathi
Publikováno v:
Synlett. 2011:1687-1692
A novel, efficient one-pot method has been developed to synthesize amphiphiles such as N-alkylated/N-allylated triethyl-amines and pyridinium salts for the first time from n-alcohols and naturally occurring terpenes (allyl alcohols) in good yields. T
Publikováno v:
Synthetic Communications. 41:1572-1583
Stilbene derivates (stilbenoids) are present in plants and show a wide range of biological activities and potential therapeutic value. In continuation of our natural product synthesis program, an efficient, simple, and practical method has been devel
Publikováno v:
Journal of Natural Products. 73:747-750
A one-pot chemical process using BF(3).Et(2)O for the synthesis of a new class of 1(15--11) abeotaxanes from normal taxanes has been developed. The chemical structures of rearranged 1(15--11) abeotaxane were established by extensive 2D NMR spectrosco
Publikováno v:
Synthesis. 2009:3791-3796
An efficient, simple, and practical method has been developed to regioselectively synthesize (E)-stilbenes and (E,E)-1,4-diphenylbuta-1,3-diene in good to excellent yields in the presence of boron trifluoride-diethyl ether complex as a catalyst in a
Publikováno v:
Synthetic Communications. 39:1949-1956
We have developed an efficient method to deacetylate the aromatic acetates using NaOAc in excellent yields and demonstrated the application of the procedure in the synthesis of natural products.
Publikováno v:
Tetrahedron Letters. 49:4409-4415
We have developed an efficient method to regioselectively deacetylate polyacetoxyacetophenones using BF 3 ·OEt 2 in excellent yields and demonstrated the application of the procedure in the synthesis of natural products.
Autor:
Tadigoppula Narender, K. Papi Reddy
Publikováno v:
Tetrahedron Letters. 48:7628-7632
In continuation of our program on synthetic chalcones, we have developed a simple and convenient method for the synthesis of chromanochalcones from prenylated chalcones in high yields by regioselective cyclization using BF 3 –Et 2 O.
Autor:
Tadigoppula Narender, K. Papi Reddy
Publikováno v:
Tetrahedron Letters. 48:3177-3180
Chalcones are secondary metabolites of terrestrial plants, precursors for the biosynthesis of flavonoids and exhibit various biological activities. Condensation of substituted acetophenones (2a–12a) with various aromatic aldehydes (1b–7b) in the
Autor:
Philip Prathipati, A. K. Srivastava, Tanvir Khaliq, K. Papi Reddy, S.C. Agarwal, Tadigoppula Narender, Kanwal Raj, Anju Puri, Priti Tiwari, Ramesh Chander, Shweta Shweta
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 17:1808-1811
The plant Aegle marmelos belongs to the family of Rutaceae. From the leaves of A. marmelos an alkaloidal-amide, Aegeline 2, was isolated and found to have antihyperglycemic activity as evidenced by lowering the blood glucose levels by 12.9% and 16.9%