Zobrazeno 1 - 9
of 9
pro vyhledávání: '"E. Kate Dorling"'
Autor:
Eric J. Thomas, Olivier Germay, Christopher J Moore, Nathaniel G. Martin, Lindsay A. Hobson, E. Kate Dorling, Matthew Booth, Anna P. Weston, Sam Donnelly, Devendra Negi, Pilar Castreno, Naresh Kumar, Christopher T. Brain
Publikováno v:
Pure and Applied Chemistry. 78:2015-2028
Allylstannanes with remote heteroatom substituents are transmetallated by tin(IV) halides to give allyltin trihalides which react with aldehydes with useful levels of remote stereocontrol; the use of this chemistry is exemplified by syntheses of seve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4436674f77536089f914fe566521d87
https://doi.org/10.1351/pac200678112015
https://doi.org/10.1351/pac200678112015
Publikováno v:
Synlett. 2001:1105-1108
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6fd23fa9813da11baf5192f79f40d78
https://doi.org/10.1055/s-2001-15145
https://doi.org/10.1055/s-2001-15145
Autor:
E. Kate Dorling, Eric J. Thomas
Publikováno v:
Tetrahedron Letters. 40:471-474
The relative configurations of 1,8-stereogenic centres can be controlled by coupling the tin(IV) chloride promoted reactions of aldehydes with 4-alkoxypent-2-enylstannanes, which proceed with excellent 1,5-induction, with an Ireland-Claisen rearrange
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff0cd29bcfb9ab2e34d2be37f40d8c21
https://doi.org/10.1016/s0040-4039(98)02427-7
https://doi.org/10.1016/s0040-4039(98)02427-7
Publikováno v:
Tetrahedron Letters. 37:263-266
We report here a convenient method for the conversion of Fmoc amino acids to their N-methylated derivatives. The method involves reaction with formaldehyde and then reduction with triethylsilane (TES). The method is particularly attractive in that th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a0302b1476ce1b8e491321b3fb3f64b
https://doi.org/10.1016/0040-4039(95)02145-0
https://doi.org/10.1016/0040-4039(95)02145-0
Publikováno v:
ChemInform. 30
The relative configurations of 1,8-stereogenic centres can be controlled by coupling the tin(IV) chloride promoted reactions of aldehydes with 4-alkoxypent-2-enylstannanes, which proceed with excellent 1,5-induction, with a 2,3-Wittig rearrangement:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81833876fcd295833a4d205550e05f0b
https://doi.org/10.1002/chin.199917272
https://doi.org/10.1002/chin.199917272
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99c2bb94b509f17dfa82f95b5968d63d
https://doi.org/10.1002/chin.200142245
https://doi.org/10.1002/chin.200142245
Autor:
Matthew Booth, Christopher Brain, Pilar Castreno, Sam Donnelly, E. Kate Dorling, Olivier Germay, Lindsay Hobson, Naresh Kumar, Nathaniel Martin, Christopher Moore, et al. et al.
Publikováno v:
ChemInform. 38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee29cee03e9db6e6de9ef8662645ef1a
https://doi.org/10.1002/chin.200717235
https://doi.org/10.1002/chin.200717235
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28f2fe7a4b977bf6410d97e4e5cf5690
https://doi.org/10.1002/chin.200045234
https://doi.org/10.1002/chin.200045234
Publikováno v:
Tetrahedron Letters. 40:475-476
The relative configurations of 1,8-stereogenic centres can be controlled by coupling the tin(IV) chloride promoted reactions of aldehydes with 4-alkoxypent-2-enylstannanes, which proceed with excellent 1,5-induction, with a 2,3-Wittig rearrangement:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcc8f4cb3629ae7f2f3366c57a42acfd
https://doi.org/10.1016/s0040-4039(98)02428-9
https://doi.org/10.1016/s0040-4039(98)02428-9