Zobrazeno 1 - 10
of 12
pro vyhledávání: '"G. Dasharatha Reddy"'
Autor:
G. Dasharatha Reddy, Michael Gahr, Eric L. Burch, Peter Gedeck, Jeffrey A. Engleman, Dario M. Bassani, Siegfried Schneider, Frederick D. Lewis, Wighard Jaeger, Bliss E. Cohen
Publikováno v:
Journal of the American Chemical Society. 117:660-669
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4260c3a01ebea4d362e47ee9b7c39344
https://doi.org/10.1021/ja00107a010
https://doi.org/10.1021/ja00107a010
Publikováno v:
Tetrahedron Letters. 35:535-538
The photosensitized electron transfer reactions of several 1- and 9-(aminoalkyl)phenanthrenes with metadicyanobenzene have been investigated. These reactions provide an efficient method of synthesis for the skeletal structures of the aporphine, phena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1607c4e6cf9c5bdf11b5a139ad144365
https://doi.org/10.1016/s0040-4039(00)75831-x
https://doi.org/10.1016/s0040-4039(00)75831-x
Publikováno v:
Journal of the American Chemical Society. 116:597-605
The photochemical and photophysical behavior of several ((N,N-dimethylamino)alkyl)styrenes in which the amino group is attached to the styrene α- or β-carbon by a methyl, ethyl, propyl, or butyl polymethylene chain has been investigated. Efficient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc34f185c5293e06ca6911d5a41d652b
https://doi.org/10.1021/ja00081a021
https://doi.org/10.1021/ja00081a021
Publikováno v:
The Journal of Organic Chemistry. 58:6390-6393
The photophysical and photochemical behavior of a series of α-[(N-methylamino)alkyl]styrenes with two to four methylenes separating the styryl and amino groups and an (aminoalkyl)indene have been investigated and the results compared to those for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2809ac7b981a616ac14fbcb8d3ab011c
https://doi.org/10.1021/jo00075a037
https://doi.org/10.1021/jo00075a037
Publikováno v:
Tetrahedron Letters. 33:4249-4252
The photochemical reactions of several ortho-(aminoalkyl)stilbenes and their N-methyl derivatives have been investigated under conditions of direct and electron-transfer sensitized irradiation and are found to provide an efficient method for the synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3851827262c366f6a7aabc3154b4257
https://doi.org/10.1016/s0040-4039(00)74230-4
https://doi.org/10.1016/s0040-4039(00)74230-4
Publikováno v:
Pure and Applied Chemistry. 64:1271-1277
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3236d56c5d21d227f7bf4f20e2e62cf3
https://doi.org/10.1351/pac199264091271
https://doi.org/10.1351/pac199264091271
Autor:
Frederick D. Lewis, Masanobu Kojima, G. Dasharatha Reddy, Julie A. Meltzer, Bruce E. Tillberg, Jeffrey E. Elbert
Publikováno v:
The Journal of Organic Chemistry. 56:5311-5318
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b71909132f5832067a340da3a2f8ccb5
https://doi.org/10.1021/jo00018a020
https://doi.org/10.1021/jo00018a020
Publikováno v:
Journal of the American Chemical Society. 113:3498-3506
The photophysical and photochemical behavior of a series of secondary and tertiary ω-(β-styryl) aminoalkanes with one to five methylenes separating the styryl and amino groups has been investigated and compared to the intermolecular reactions of 1-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::114a120f7c8aff3ed4691e1f6fb8458b
https://doi.org/10.1021/ja00009a041
https://doi.org/10.1021/ja00009a041
Publikováno v:
Journal of the American Chemical Society. 115:6468-6469
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68176afaaccd881d475a239bf0de460c
https://doi.org/10.1021/ja00067a095
https://doi.org/10.1021/ja00067a095
Publikováno v:
Journal of the American Chemical Society. 111:6465-6466
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c10e03f088fc844c3b6cd4e741344438
https://doi.org/10.1021/ja00198a091
https://doi.org/10.1021/ja00198a091