Zobrazeno 1 - 10
of 716
pro vyhledávání: '"Douglass F. Taber and"'
Publikováno v:
Chemistry – A European Journal. 27:11773-11794
The Pd-catalyzed carbon-carbon bond formation pioneered by Heck in 1969 has dominated medicinal chemistry development for the ensuing fifty years. As the demand for more complex three-dimensional active pharmaceuticals continues to increase, preparat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10cc72b480c355fce552be9fdb5051ef
https://doi.org/10.1002/chem.202101232
https://doi.org/10.1002/chem.202101232
Autor:
Douglass F. Taber
Covalent bonds are fluid, not rigid, as with hand-held plastic models. Raspberry jam is an effective visual demonstration of this fluidity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51f28e3194f455791f5f00ec287f9d37
https://doi.org/10.33774/chemrxiv-2021-2vwc1
https://doi.org/10.33774/chemrxiv-2021-2vwc1
Publikováno v:
Chemistry – A European Journal. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16d613198bf8ea6bfc4fa9f1de071559
https://doi.org/10.1002/chem.202184662
https://doi.org/10.1002/chem.202184662
Autor:
Douglass F. Taber
Using 13C NMR data that includes 1H coupling allows sophomore organic students to solve simple structural problems, even early in the first semester of the sophomore organic course.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8cf7c23f48b835af0cf5b47ca7b0a20
https://doi.org/10.33774/chemrxiv-2021-gh36l
https://doi.org/10.33774/chemrxiv-2021-gh36l
Autor:
Michael J. Hennessy, Krishna Raman, Robert E. Ruckle, Jonathan S. Schuchardt, Douglass F. Taber, R. Scott Hoerrne
Publikováno v:
Catalysis of Organic Reactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::143759c69e43294786e744a5666c0247
https://doi.org/10.1201/9781003066446-5
https://doi.org/10.1201/9781003066446-5
Autor:
Douglass F. Taber
Publikováno v:
Israel Journal of Chemistry. 58:11-17
An overview of the development of modern organic synthesis is given. Key researchers and their work are highlighted with a focus on the development of analytical and synthetic techniques currently in use.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::450e9896530d43a5cf61a0c919f54167
https://doi.org/10.1002/ijch.201500006
https://doi.org/10.1002/ijch.201500006
Publikováno v:
Tetrahedron. 71:139-146
A simple protocol has been established for the preparation of a family of crystalline N-aryl γ-hydroxycrotonamides, useful four-carbon synthons. These were further elaborated to analogs of monastrol having variant ester sidechains, that were evaluat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4dd3bd03b66e5a35e35de140e2656a1
https://doi.org/10.1016/j.tet.2014.11.022
https://doi.org/10.1016/j.tet.2014.11.022
Autor:
Douglass F. Taber
Publikováno v:
Organic Synthesis
Hiromitsu Takayama of Chiba University used (Org. Lett. 2014, 16, 5000) the Itsuno-Corey protocol to reduce the enone 1 to the allylic alcohol 2. Peiming Gu of Ningxia University developed (Org. Lett. 2014, 16, 5339) a Cu catalyst that cyclized the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff760c2274eeeb21b713ef11693eb027
https://doi.org/10.1093/oso/9780190646165.003.0034
https://doi.org/10.1093/oso/9780190646165.003.0034
Autor:
Douglass F. Taber
Publikováno v:
Organic Synthesis
Shaorong Yang and Huanfeng Jiang of the South China University of Technology assembled (Angew. Chem. Int. Ed. 2014, 53, 7219) the β-lactone 3 by the Pd-catalyzed addition of 2 to the alkyne 1. Jack R. Norton of Columbia University observed (J. Am. C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06c0fdecc1579cc2d2a21298046bdf0d
https://doi.org/10.1093/oso/9780190646165.003.0047
https://doi.org/10.1093/oso/9780190646165.003.0047
Autor:
Douglass F. Taber
Publikováno v:
Organic Synthesis
Hisashi Yamamoto of the University of Chicago and Chubu University developed (J. Am. Chem. Soc. 2014, 136, 1222) a tungsten catalyst for the enantioselective oxidation of allylic alcohols such as 1 to the epoxide 2. Homoallylic alcohols also worked
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb43bc3a6e8e92386d0d77b1d0273020
https://doi.org/10.1093/oso/9780190646165.003.0041
https://doi.org/10.1093/oso/9780190646165.003.0041