Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kaliappan Iyanar"'
Autor:
Kaliappan Iyanar, Jessica D. Dietz, Graciela B. Arhancet, Horng-Chih Huang, Danny J. Garland, Marcia I. Heron, Silvia I. Pomposiello, Xiao Hu, Len F. Lee, Joe T. Collins, Scott S. Woodard, James Robert Blinn, Maria A. Payne, Brenda L. Case, Rhonda S. Woerndle
Publikováno v:
Journal of Medicinal Chemistry. 53:5970-5978
A new 1,4-dihydropyridine 5a, containing a cyano group at the C3 position, was recently reported to possess excellent mineralocorticoid receptor (MR) antagonist in vitro potency and no calcium channel-blocker (CCB) activity. In the present study, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9288e4053ed7e7f775bce265c4ec3184
https://doi.org/10.1021/jm100506y
https://doi.org/10.1021/jm100506y
Autor:
Grace M. Wagner, Joe T. Collins, Scott S. Woodard, Randal E Numann, Kaliappan Iyanar, Graciela B. Arhancet, Danny J. Garland, James Robert Blinn, Jessica D. Dietz, Horng-Chih Huang, Xiao Hu
Publikováno v:
Journal of Medicinal Chemistry. 53:4300-4304
A number of known 1,4-dihydropyridine CCBs were identified as having comparable potency to the steroidal MR antagonist eplerenone. Chiral resolution of mebudipine revealed that MR and CCB activity reside in opposite enantiomers. Small molecule X-ray
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6e7af97f6c33d3bb740cfc75d288cac
https://doi.org/10.1021/jm1002827
https://doi.org/10.1021/jm1002827
Autor:
Kaliappan Iyanar, Robert W. Murray
Publikováno v:
Heteroatom Chemistry. 9:347-350
Some secondary amines of varying structural type have been oxidized by the methyltrioxorhenium/hydrogen peroxide system to the corresponding nitroxides in excellent yield. These results, coupled with our earlier work using this system, indicate the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dfbb6f515f5942888fa6f4f9ae9cf60
https://doi.org/10.1002/(sici)1098-1071(1998)9:3<347::aid-hc12>3.0.co
https://doi.org/10.1002/(sici)1098-1071(1998)9:3<347::aid-hc12>3.0.co
Autor:
Robert W. Murray, Kaliappan Iyanar
Publikováno v:
Tetrahedron Letters. 38:335-338
Methyltrioxorhenium catalyzes the oxidation of C 60 by hydrogen peroxide to give C 60 O. The reaction continues to produce C 60 O 2 and higher oxides. The yield of C 60 O represents a modest improvement over that given by other methods. The reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ef6e46f119a903ddf3bf1ce258b7241
https://doi.org/10.1016/s0040-4039(96)02345-3
https://doi.org/10.1016/s0040-4039(96)02345-3
Publikováno v:
Tetrahedron Letters. 37:805-808
Methyltrioxorhenium catalyzes the reaction of hydrogen peroxide with organonitrogen compounds. The reactions are facile and high yield at room temperature or below. The observed chemistry is similar to that previously described by us using dimethyldi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bedf5829fb404807358ae54392b8013
https://doi.org/10.1016/0040-4039(95)02326-7
https://doi.org/10.1016/0040-4039(95)02326-7
Publikováno v:
Tetrahedron Letters. 36:6415-6418
Methyltrioxorhenium catalyzes the CH insertion reaction of hydrocarbons by hydrogen peroxide. In suitable substrates the reaction is stereospecific with retention.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b71d148a64444d9f22efc63b3b0bd971
https://doi.org/10.1016/0040-4039(95)01344-h
https://doi.org/10.1016/0040-4039(95)01344-h
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b60c54b44d36f4ff916936a0f78c8ed7
https://doi.org/10.1002/chin.199603049
https://doi.org/10.1002/chin.199603049
Publikováno v:
ChemInform. 27
Methyltrioxorhenium catalyzes the reaction of hydrogen peroxide with organonitrogen compounds. The reactions are facile and high yield at room temperature or below. The observed chemistry is similar to that previously described by us using dimethyldi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57d33e221cdbf35d7a4fadcec2882363
https://doi.org/10.1002/chin.199622064
https://doi.org/10.1002/chin.199622064
Publikováno v:
ChemInform. 28
Secondary amines are oxidized by the methyltrioxorhenium/hydrogen peroxide system to the corresponding nitrones in excellent yield. The results provide a further example of the parallel between the chemistry of this metal system and that of the dioxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee722b29da9cf6002a3c51470ecf5cbc
https://doi.org/10.1002/chin.199716075
https://doi.org/10.1002/chin.199716075
Autor:
Kaliappan Iyanar, Robert W. Murray
Publikováno v:
ChemInform. 29
Some secondary amines of varying structural type have been oxidized by the methyltrioxorhenium/hydrogen peroxide system to the corresponding nitroxides in excellent yield. These results, coupled with our earlier work using this system, indicate the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12fe125c1343e6ce7a956df46c174ee5
https://doi.org/10.1002/chin.199832062
https://doi.org/10.1002/chin.199832062