Zobrazeno 1 - 10
of 59
pro vyhledávání: '"David H. Grayson"'
Autor:
Mathias C. Eichler, David H. Grayson
Publikováno v:
ARKIVOC, Vol 2014, Iss 6, Pp 38-53 (2014)
Externí odkaz:
https://doaj.org/article/59f0cd15548148049dffa6655be29de3
Publikováno v:
ARKIVOC, Vol 2014, Iss 2, Pp 161-174 (2013)
Externí odkaz:
https://doaj.org/article/378010d9ffea4ac19c4edd7f2bd9f53e
Autor:
David H. Grayson, Stephen H. O’Donnell
Publikováno v:
ARKIVOC, Vol 2003, Iss 7, Pp 4-14 (2002)
Externí odkaz:
https://doaj.org/article/42c43bfd3cf042b289e906cda3134e26
Autor:
Jerome Fakhry, David H. Grayson
Publikováno v:
Tetrahedron. 74:556-563
Phenyl benzenethiosulfinate reacts with enolate anions derived from ketones to give α-phenylsulfinyl ketones directly, together with minor amounts of α-phenylsulfanyl ketones. These are easily separated by forming the water-soluble sodium salts of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a2508054078e401b243ed7df5b05c4e
https://doi.org/10.1016/j.tet.2017.12.028
https://doi.org/10.1016/j.tet.2017.12.028
Autor:
David H. Grayson, Mathias C. Eichler
Publikováno v:
ARKIVOC, Vol 2014, Iss 6, Pp 38-53 (2014)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d8ba92debce3492cad69c45a5dc4e5f
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p008.843
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p008.843
Publikováno v:
Tetrahedron. 70:7241-7244
Deprotonation of diethyl (2-carboethoxy)benzylphosphonate using sodium ethoxide followed by reaction of the carbanion with furfural or aryl aldehydes gives diethyl (E)-1-(2′-carboxyphenyl)-1-phosphono-2-arylethenes that are formed via intramolecula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f13655b724ccca2a0deac128f16fd1e8
https://doi.org/10.1016/j.tet.2014.07.001
https://doi.org/10.1016/j.tet.2014.07.001
Autor:
Eva M. Gallagher, David H. Grayson
Publikováno v:
ARKIVOC, Vol 2014, Iss 5, Pp 420-429 (2014)
E)-3-Bromo-1-phenylsulfonylprop-1-ene and (E)-3-iodo-1-phenylsulfonylprop-1-ene both form allylic organozinc reagents that react with aromatic aldehydes to give mainly 4-aryl-4-hydroxy1-phenylsulfonylbut-1-enes. In contrast, reactions of the same org
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da4528d35e214b2822607cebf35b63d3
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p008.741
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p008.741
Publikováno v:
European Journal of Organic Chemistry. 2014:3565-3569
A novel method for the synthesis of aryl-substituted guanidines in good overall yields is presented; it consists of the acidic cleavage of 2-(arylamino)-4,6-dimethoxypyrimidines, which were prepared by coupling aryl bromides with 2-amino-4,6-dimethox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7830149c82383bf6f7d1fadbd7e00cae
https://doi.org/10.1002/ejoc.201402179
https://doi.org/10.1002/ejoc.201402179
Publikováno v:
Tetrahedron Letters. 56:4990-4992
The use of 2-chloro-4,6-dimethoxypyrimdine as a tool for the syntheses of substituted guanidines is presented. This method, that we had previously shown to be very useful for aromatic amines, introduces an atom economical, cost effective and environm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3476a280edeace41c3a996baf742609
https://doi.org/10.1016/j.tetlet.2015.07.007
https://doi.org/10.1016/j.tetlet.2015.07.007
Autor:
David H. Grayson, Frank W. Lewis
Publikováno v:
Tetrahedron: Asymmetry. 23:643-649
Some camphor-derived vinyl sulfones bearing an oxygen functionality at the allylic position have been synthesised and their nucleophilic epoxidation reactions under Meth-Cohn conditions have been explored. The γ-oxygenated camphor-derived vinyl sulf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99c4afb8d53e04b882049d0661b4a913
https://doi.org/10.1016/j.tetasy.2012.04.014
https://doi.org/10.1016/j.tetasy.2012.04.014