Zobrazeno 1 - 6
of 6
pro vyhledávání: '"John C. Keeler"'
Autor:
Padmanava Pradhan, Kathryn A. Thomasson, Mahesh K. Lakshman, John H. Hilmer, Barbara Zajc, John C. Keeler, Felix N. Ngassa
Publikováno v:
Journal of the American Chemical Society. 129:68-76
A diastereoselective synthesis of the nucleoside adducts corresponding to a cis ring-opening of the carcinogen (+/-)-7 beta, 8 alpha-dihydroxy-9 alpha,10 alpha-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene (BaP DE-2) by 2'-deoxyadenosine and 2'-deoxyguanos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::280d23571a6e3343ae422467bbeb196a
https://doi.org/10.1021/ja063902u
https://doi.org/10.1021/ja063902u
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ad00c001830abfdefebb50767eeb371
https://doi.org/10.1002/chin.199940194
https://doi.org/10.1002/chin.199940194
Autor:
Larry M. Russon, Mahesh K. Lakshman, Yen Q. V. Dinh, John C. Keeler, John H. Hilmer, Felix N. Ngassa
Publikováno v:
ChemInform. 31
The 3‘,5‘-bis-O-TBDMS derivative of 2‘-deoxyguanosine can be converted to its O6-alkyl and O6-aryl ethers as well as to N6-substituted diaminopurine nucleosides in two simple steps. Also described is a novel, nonaqueous, one-step O6-desulfonyla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ad78c37570761a301189d0d7142cfba
https://doi.org/10.1002/chin.200027214
https://doi.org/10.1002/chin.200027214
Autor:
Mahesh K. Lakshman, Larry M. Russon, John H. Hilmer, Felix N. Ngassa, Yen Q. V. Dinh, Jocelyn Q. Martin, John C. Keeler
Publikováno v:
ChemInform. 32
Suzuki−Miyaura cross-coupling of haloaromatic compounds with arylboronic acids provides a simple entry to biaryl systems. Despite its ease, to date, there are no detailed investigations of this pro...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17c034a5fc7fd41c3ffa6f4172d9712f
https://doi.org/10.1002/chin.200150204
https://doi.org/10.1002/chin.200150204
Autor:
Jocelyn Q. Martin, Felix N. Ngassa, John H. Hilmer, Mahesh K. Lakshman, John C. Keeler, Larry M. Russon, Yen Q. V. Dinh
Publikováno v:
Journal of the American Chemical Society. 123(32)
Suzuki-Miyaura cross-coupling of haloaromatic compounds with arylboronic acids provides a simple entry to biaryl systems. Despite its ease, to date, there are no detailed investigations of this procedure for deoxynucleoside modification. As shown in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34af982ebf1cd51e52e75624226e60b9
https://pubmed.ncbi.nlm.nih.gov/11493051
https://pubmed.ncbi.nlm.nih.gov/11493051
Publikováno v:
Journal of the American Chemical Society. 121:6090-6091
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b8b177b06e4ab771511022f4b4eda4d
https://doi.org/10.1021/ja9908671
https://doi.org/10.1021/ja9908671