Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Kenneth J. O'Connor"'
Publikováno v:
Journal of Chemical Education. 88:325-327
Hydrogenation of alkenes is an important reaction in the synthesis of organic molecules. In this experiment, students conduct a high-yield microscale hydrogenation reaction of methyl trans-cinnamate using a readily available, safe, and convenient hyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa1a54cace999ba5897e5ba49f1f6b81
https://doi.org/10.1021/ed1007475
https://doi.org/10.1021/ed1007475
Publikováno v:
Stress (Amsterdam, Netherlands). 14(5)
This study was designed to assess physiological and behavioral correlates of academic stress during a college course in organic chemistry in the USA. Participants (45 females, 46 males, mean age 19.88 years) were screened for their basal hypothalamic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2ee23373a4aadbd0c3866d10fc198bb
https://pubmed.ncbi.nlm.nih.gov/21682652
https://pubmed.ncbi.nlm.nih.gov/21682652
Publikováno v:
Tetrahedron Letters. 34:1905-1908
Highly pure (S)-1.1-di(p-anisyl)-3-methyl-1,2-butane diamine (valinyl diamine), 4a and 1,1-di(p-anisyl)-2-propane diamine (alaninyl dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77e1b9cd557b0eb849deb4a65cfa4913
https://doi.org/10.1016/s0040-4039(00)91959-2
https://doi.org/10.1016/s0040-4039(00)91959-2
Publikováno v:
ChemInform. 22
As a result of this and previous research in this area, we view macrocyclic Ni II complexes as versatile catalysts for a wide variety of synthetically useful transformations. In addition to catalyzing the epoxidation of olefins with high turnover num
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c528a2b95bebafa1f3111f81a7407952
https://doi.org/10.1002/chin.199125140
https://doi.org/10.1002/chin.199125140
Publikováno v:
ChemInform. 23
New chiral metal salen complexes substituted in the 3 position with bulky silyl groups (TMS, TBDMS) have been synthesized. Although some of these complexes catalyzed the epoxidation of unfunctionalized olefins in moderate to high ee's, they catalyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::148b30827d8822dcdbfc439db9352d00
https://doi.org/10.1002/chin.199237060
https://doi.org/10.1002/chin.199237060
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc6c4d6c147fa1bb84976c447940d971
https://doi.org/10.1002/chin.199333238
https://doi.org/10.1002/chin.199333238
Publikováno v:
Tetrahedron Letters. 33:1001-1004
New chiral metal salen complexes substituted in the 3 position with bulky silyl groups (TMS, TBDMS) have been synthesized. Although some of these complexes catalyzed the epoxidation of unfunctionalized olefins in moderate to high ee's, they catalyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d501d9487aa1671605b0e1f98c97c62
https://doi.org/10.1016/s0040-4039(00)91844-6
https://doi.org/10.1016/s0040-4039(00)91844-6
Publikováno v:
Journal of the American Chemical Society. 112:4568-4570
Transition-metal-catalyzed transfer of oxygen atoms to organic substrates is of interest in the study of bioinorganic mechanisms and the development of efficient catalysts for laboratory and industrial organic synthesis. Certain nickel(II) catalysts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a731c92a5fed24c7eafcdcf7ebc0286
https://doi.org/10.1021/ja00167a078
https://doi.org/10.1021/ja00167a078
Publikováno v:
Tetrahedron Letters. 30:3271-3274
The stability and reactivity of vinyl titanium triisopropoxides having a variety of substitution patterns has been explored. These reagents when prepared in Et2O have proven to be more stable than expected based on prior reports, and they exhibit suf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9aa904e143d2350d6559c0fea486c5c8
https://doi.org/10.1016/s0040-4039(00)99219-0
https://doi.org/10.1016/s0040-4039(00)99219-0