Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Wayne F. K. Schnatter"'
Publikováno v:
The Journal of Physical Chemistry A. 117:13079-13088
There are still some secrets left to this well-studied reaction. Previously unreported relationships discovered are as follows. The ordering of reactivities of C6H5X is the same as that of enthalpies of hydrogenation of the ring to the correspondingl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3e076655f022ff16925a9a7b2fccd04
https://doi.org/10.1021/jp409623j
https://doi.org/10.1021/jp409623j
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 21(29)
Although electrophilic addition to alkenes has been well studied, some secrets still remain. Halogenations, hydrohalogenations, halohydrin formations, hydrations, epoxidations, other oxidations, carbene additions, and ozonolyses are investigated to e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6155cabea55e4f4f38d530288d058f43
https://pubmed.ncbi.nlm.nih.gov/25959409
https://pubmed.ncbi.nlm.nih.gov/25959409
Publikováno v:
ChemInform. 23
The uniquely hydrocarbon-like capped porphyrin (C70H68N4), 1i, has been successfully prepared by a high dilution reaction of pyrrole with tetrakis-1,2,4,5-[pentyl-5′-(2″-formylphenyl)]-benzene 1h in the presence of boron trifluoride etherate. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b512eee27e28f7a94fd92801aa9722c9
https://doi.org/10.1002/chin.199209174
https://doi.org/10.1002/chin.199209174
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9803ed866562ee8528e29ee2a49c1aa
https://doi.org/10.1002/chin.199405148
https://doi.org/10.1002/chin.199405148
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3c0d49c73ac436311aad68504a7b6e9
https://doi.org/10.1002/chin.199440251
https://doi.org/10.1002/chin.199440251
Autor:
Abhijit Mitra, Charles Shimanskas, Wayne F. K. Schnatter, Kirstin F. Warner, Ammiel Bachrach, Atiq-ur Rehman
Publikováno v:
ChemInform. 30
Herein, we report a new and efficient method for the large scale synthesis of 2,6-dicarboxyfluorenone 5 in 95% yield using 0.01mol% of bis(triphenylphosphine)palladium(II) chloride, (PPh3)2 PdCl2, as a catalyst, starting with the reaction of 2,5-dime
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27b68dba08ae2152dde0b7491beed9c4
https://doi.org/10.1002/chin.199917110
https://doi.org/10.1002/chin.199917110
Publikováno v:
ChemInform. 30
The reaction of gem-dihalides with Na2Fe(CO)4 results in the formation of alkenes instead of the iron(0) carbene complexes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b052eb46372d8924cf664027890c09ea
https://doi.org/10.1002/chin.199951067
https://doi.org/10.1002/chin.199951067
Autor:
Nikita Matsunaga, Wayne F. K. Schnatter, Lazaros Kakalis, Vioela Caze, Jimmy Truong, Gayatri K. Joshi, Ravish K. Akhani
Publikováno v:
ChemInform. 41
1-chloroalkynes and 1-bromohexyne undergo cycloaddition reactions with ethoxyvinylketeneiron(0) complexes to form chloro and bromocatechols. With most substituents, the halogen is incorporated ortho to the phenolic hydroxyl group regioselectively. Wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a6b0fad1aa58a381ae8ac5c02c66cad
https://doi.org/10.1002/chin.201019067
https://doi.org/10.1002/chin.201019067
Autor:
Jimmy Truong, Vioela Caze, Nikita Matsunaga, Lazaros Kakalis, Gayatri K. Joshi, Ravish K. Akhani, Wayne F. K. Schnatter
1-chloroalkynes and 1-bromohexyne undergo cycloaddition reactions with ethoxyvinylketeneiron(0) complexes to form chloro and bromocatechols. With most substituents, the halogen is incorporated ortho to the phenolic hydroxyl group regioselectively. Wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e156ce54892cf711a5a6d70e155ad061
https://europepmc.org/articles/PMC2811311/
https://europepmc.org/articles/PMC2811311/
Publikováno v:
Tetrahedron letters. 50
Reaction of iron(0) carbene complexes with hexafluorobut-2-yne produces 3,4-bis(trifluoromethylated)furans in a process that is favored for electron rich carbenes. No traces of furannulation or benzannulation are observed with Group 6 Fischer carbene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e5b6522037697d0873f8a45cb6d382f
https://pubmed.ncbi.nlm.nih.gov/20046214
https://pubmed.ncbi.nlm.nih.gov/20046214