Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Tamilselvan Rajasekaran"'
Autor:
Tamilselvan Rajasekaran, Graeme C. Freestone, Rodrigo Galindo-Murillo, Barbara Lugato, Hans Gaus, Michael T. Migawa, Eric. E. Swayze, Thomas E. Cheatham, Punit P. Seth, Stephen Hanessian
Publikováno v:
The Journal of Organic Chemistry. 88:3599-3614
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34b43ee8621b506c8e97b1ef94a57433
https://doi.org/10.1021/acs.joc.2c02796
https://doi.org/10.1021/acs.joc.2c02796
Autor:
Tamilselvan Rajasekaran, Graeme C. Freestone, Rodrigo Galindo-Murillo, Barbara Lugato, Lorena Rico, Juan C. Salinas, Hans Gaus, Michael T. Migawa, Eric E. Swayze, Thomas E. Cheatham, Stephen Hanessian, Punit P. Seth
Publikováno v:
J Am Chem Soc
Journal of the American Chemical Society, vol 144, iss 4
Journal of the American Chemical Society, vol 144, iss 4
The binding affinity of therapeutic oligonucleotides (ONs) for their cognate RNA is determined by the rates of association (ka) and dissociation (kd). Single-stranded ONs are highly flexible and can adopt multiple conformations in solution, some of w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd9b42e50480f4d847f71a556cb14fdc
https://doi.org/10.1021/jacs.1c12323
https://doi.org/10.1021/jacs.1c12323
Publikováno v:
Tetrahedron. 72:2102-2108
A three-component coupling (3CC) of aryldiazoacetate, aldehyde and N-tosylimine has been achieved using 1 mol % of Rh2(OAc)4 for the synthesis of highly substituted triaryl-1,3-oxazolidines in good yields with high diastereoselectivity. This protocol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c0ab411ca931c695b3af7c1112e0ecb
https://doi.org/10.1016/j.tet.2016.02.055
https://doi.org/10.1016/j.tet.2016.02.055
Publikováno v:
European Journal of Organic Chemistry. 2015:2038-2041
The three-component coupling (3CC) of α-diazoamide, aldehyde and 3-arylideneoxindole using 5 mol-% of Rh2(OAc)4 is described to afford a novel class of dispirooxindole derivatives with complete regio- and stereoselectivity. It is a first report on t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d92667fb1b76e3e0b244b9e31e8fb458
https://doi.org/10.1002/ejoc.201500002
https://doi.org/10.1002/ejoc.201500002
Publikováno v:
Tetrahedron Letters. 55:7064-7067
A novel series of spirooxindolylcyclopropane derivatives have been synthesized in high yields from 3-diazooxindole and electron deficient olefins under catalyst/solvent-free conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::447bc92c0090d3d349078221ef2051b3
https://doi.org/10.1016/j.tetlet.2014.10.137
https://doi.org/10.1016/j.tetlet.2014.10.137
Publikováno v:
Tetrahedron. 70:8148-8154
A highly regio- and stereoselective method has been developed for the synthesis of spiro[furo[3,4-c]chromene-1,3′-indoline]-2′,4(9bH)-dione derivatives via a three component reaction of cyclic diazoamide and aldehyde with methyl 2-oxo-2H-chromene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29c9dbdb9244269c3935029b21e35664
https://doi.org/10.1016/j.tet.2014.07.093
https://doi.org/10.1016/j.tet.2014.07.093
Autor:
Govindaraju Karthik, B. Sridhar, S. Kiran Kumar, Tamilselvan Rajasekaran, Basi V. Subba Reddy
Publikováno v:
European Journal of Organic Chemistry. 2014:2221-2224
A stereoselective synthesis of oxindole-derived α-alkoxy-β-amino acid derivatives was achieved in high yield with excellent diastereoselectivity through the three-component reaction of methyl 2-diazoarylacetate, aryl alcohols, and isatin-derived ke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7881639ff76755ebf3a65e0d3686028
https://doi.org/10.1002/ejoc.201301775
https://doi.org/10.1002/ejoc.201301775
Publikováno v:
Organic Letters. 15:1512-1515
A highly stereo-, regio-, and chemoselective method has been devised for the synthesis of a wide range of spirooxindolyl oxazolidines via an intermolecular 1,3-dipolar cycloaddition of carbonyl ylides generated from dimethyl diazomalonate and aromati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::548adbee777b225c48a0ecd0b8f4d7d5
https://doi.org/10.1021/ol400287q
https://doi.org/10.1021/ol400287q
Publikováno v:
ChemInform. 47
A three-component coupling (3CC) of aryldiazoacetate, aldehyde and N-tosylimine has been achieved using 1 mol % of Rh2(OAc)4 for the synthesis of highly substituted triaryl-1,3-oxazolidines in good yields with high diastereoselectivity. This protocol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7cfda132f1a8c6a92d6213b792de5aa
https://doi.org/10.1002/chin.201632136
https://doi.org/10.1002/chin.201632136
Publikováno v:
Tetrahedron Letters. 53:3416-3420
Rhodium(II) acetate catalyzed intermolecular cyclopropanation of glycals with cyclic carbenoids generated from 3-diazo-2-oxindole has been achieved to produce a novel series of spirooxindolyl sugar derivatives in good yields under mild experimental c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a12907e6c1fd658eda3a78c0ea09151
https://doi.org/10.1016/j.tetlet.2012.04.031
https://doi.org/10.1016/j.tetlet.2012.04.031