Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Chinnasamy Ramaraj, Ramanathan"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 428-440 (2017)
An efficient and alternative synthetic approach has been developed to prepare various N-(arylethyl)piperazine-2,6-diones from 4-benzenesulfonyliminodiacetic acid and primary amines using carbonyldiimidazole in the presence of a catalytic amount of DM
Externí odkaz:
https://doaj.org/article/332f47d2ce9741cb883b4adcd4c0e07c
Autor:
Sheikh Haider Ali, Anita Sahani, Sumanta Pradhan, Chinnasamy Ramaraj Ramanathan, Ramana Sreenivasa Rao
Publikováno v:
Journal of Heterocyclic Chemistry. 58:1415-1428
Autor:
Savarimuthu Philip Anthony, Edwin Konikkara Abi, Chinnasamy Ramaraj Ramanathan, Nagamalla Someshwar, Muthupandi Karthick
Publikováno v:
Organic & Biomolecular Chemistry. 18:8653-8667
ortho-Quinone methides, very reactive transient intermediates, are utilized successfully in synthesizing complex organic molecules of natural and biological significance. Among several synthetic protocols, the acid catalyzed generation of ortho-quino
Autor:
R. Padmanaban, Muthupandi Karthick, Chinnasamy Ramaraj Ramanathan, Kesa Venkatanna, Santhakumar Yeswanth Kumar
Publikováno v:
Organic & Biomolecular Chemistry. 17:4077-4086
A conformationally rigid chiral bicyclic skeleton tethered bipyridine–Zn(OTf)2 complex facilitated the enantioselective Friedel–Crafts alkylation of indoles with trans-β-nitroarylalkenes in an enantioselective manner at elevated temperature. Ind
Autor:
Chinnasamy Ramaraj Ramanathan, Ramana Sreenivasa Rao, Anita Sahani, Adithya Vadakkayil, Muthupandi Karthick, Mahalingam Mummoorthi, Murugesan Santhosh
Publikováno v:
Journal of Chemical Sciences. 133
Niobium pentoxide, a bifunctional solid surface catalyst, has been successfully employed to facilitate the three-component reaction between aldehydes, amines and triethyl phosphite at room temperature under solvent-free conditions to generate α-amin
Autor:
Muthupandi, Karthick, Edwin, Konikkara Abi, Nagamalla, Someshwar, Savarimuthu Philip, Anthony, Chinnasamy Ramaraj, Ramanathan
Publikováno v:
Organicbiomolecular chemistry. 18(42)
ortho-Quinone methides, very reactive transient intermediates, are utilized successfully in synthesizing complex organic molecules of natural and biological significance. Among several synthetic protocols, the acid catalyzed generation of ortho-quino
Publikováno v:
Tetrahedron Letters. 58:3650-3653
Allylation of 2-aminophenol-derived aldimines using allyltrichlorosilane under catalyst free conditions has been developed. This reaction afforded the corresponding homoallylic amines in good to excellent yields (68–94%). The salicylaldehyde-derive
Publikováno v:
Synlett. 28:2253-2261
A simple and an efficient method for the synthesis of 7-arylfluorenes by intramolecular cyclization of the corresponding triarylcarbinols in the presence of the solid-acid catalyst NaHSO4/SiO2 has been developed. By using this method, a new chiral di
Publikováno v:
Journal of Chemical Sciences. 129:679-690
A facile and convenient method for the synthesis of substituted 2-(isoquinolin-1-yl)benzoic acids from isoindoloisoquinolinones in the presence of molecular iodine under sealed tube condition at 100 $$^{\circ }\hbox {C}$$ has been developed. This met
Publikováno v:
Tetrahedron: Asymmetry. 28:830-836
A conformationally rigid chiral molecule LB-I with Lewis basic site has been designed and synthesized in racemic form from ferrocene via Lewis acid mediated diastereoselective cyclization of hydroxy lactam. Both isomers were successfully obtained in