Zobrazeno 1 - 10
of 24
pro vyhledávání: '"M. J. Earle"'
Publikováno v:
Tetrahedron. 49:4015-4034
Reactions of N,N-dimethylformamide and N-methylformanilide with pyrophosphoryl chloride lead to the formation of reagents that undergo reactions with a wide range of nucleophilic aromatic substrates, including indoles, pyrroles, thiophenes, furans, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6550dfd8755276bf5d33ed2036219af8
https://doi.org/10.1016/s0040-4020(01)89915-4
https://doi.org/10.1016/s0040-4020(01)89915-4
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d5da62a2a7e8b16ca77aea5edc7743e
https://doi.org/10.1002/chin.199130158
https://doi.org/10.1002/chin.199130158
Autor:
M. J. Earle, Robin Alec Fairhurst, Harry Heaney, Robert F. Wilkins, Mark S. Cooper, George Papageorgiou
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6d4c6a083cba6d0d6628c1ada5178dd
https://doi.org/10.1002/chin.199111196
https://doi.org/10.1002/chin.199111196
ChemInform Abstract: Diastereoselective Reactions of Trialkylsilyl Enol Ethers with Acyliminium Ions
Autor:
George Papageorgiou, David S. Brown, Stephen C. Eyley, Robert F. Wilkins, M. J. Earle, Harry Heaney, Robin Alec Fairhurst
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca358fc959b535de0ffc5ded1bb23e90
https://doi.org/10.1002/chin.199112162
https://doi.org/10.1002/chin.199112162
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ba8232792f20b2a92e9f2d350278868
https://doi.org/10.1002/chin.199111131
https://doi.org/10.1002/chin.199111131
Autor:
Khamis F. Shuhaibar, Stephen C. Eyley, F. Ince, M. J. Earle, Robin Alec Fairhurst, Harry Heaney, G. K. Cheung
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea04921a6a7b5035e409ccbdb7164690
https://doi.org/10.1002/chin.199217184
https://doi.org/10.1002/chin.199217184
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52348b662fe13cc79fdf2dc27e863fab
https://doi.org/10.1002/chin.199217098
https://doi.org/10.1002/chin.199217098
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2860f5c978d83bc7307d306c599ca4b4
https://doi.org/10.1002/chin.199226096
https://doi.org/10.1002/chin.199226096
Autor:
Khamis F. Shuhaibar, Ian M. Downie, M. J. Earle, D. Thomas, M. F. S. Matough, G. K. Cheung, Harry Heaney
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::856e334e1b7fc3eb6963009abebf5ae5
https://doi.org/10.1002/chin.199232108
https://doi.org/10.1002/chin.199232108
Publikováno v:
ChemInform. 23
The reaction of selenium tetrachloride with the dichlorothiophene diselenolate 3,4-C4Cl2S(SeLi)2 gives triselenole (I) in 38% yield. Purification of I is difficult due to the occurrence of a facile decomposition on attempted dissolution in a variety
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0338283b0bf9ba8b5074fbc4ba049f52
https://doi.org/10.1002/chin.199228224
https://doi.org/10.1002/chin.199228224