Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Guillaume Gauron"'
Autor:
Jason D. Williams, Günter Tekautz, Philippe M. C. Roth, C. Oliver Kappe, Marc Winter, Alexander Steiner, Franz J. Strauss, Guillaume Gauron
Publikováno v:
Organic Process Research & Development. 24:2208-2216
Although continuous flow technology can facilitate the scale-up of photochemical processes it is not yet routinely implemented on production scale in the fine chemical industries. This can be attri...
Publikováno v:
ChemInform. 39
Herein we report a microwave-assisted version of a domino protocol, providing ready access to a wide variety of complex oxygen heterocycles. The latter can be converted to stereochemically, well-defined, variously substituted carbocycles, since react
Publikováno v:
ChemInform. 39
A stereoselective synthesis of heavily functionalized six-membered ring subunits, which possess functionality at sites appropriate for further elaboration, is described. The cyclopentanone moiety of hydrindenediol is required to achieve total facial
Publikováno v:
Tetrahedron: Asymmetry
Tetrahedron: Asymmetry, Elsevier, 2008, 19 (14), pp.1730-1743. ⟨10.1016/j.tetasy.2008.06.026⟩
Tetrahedron: Asymmetry, Elsevier, 2008, 19 (14), pp.1730-1743. ⟨10.1016/j.tetasy.2008.06.026⟩
Herein we report a microwave-assisted version of a domino protocol, providing ready access to a wide variety of complex oxygen heterocycles. The latter can be converted to stereochemically, well-defined, variously substituted carbocycles, since react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72d3657805d771c177a404579d795919
https://hal.archives-ouvertes.fr/hal-00326319
https://hal.archives-ouvertes.fr/hal-00326319
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2007, 9 (23), pp.4745-8. ⟨10.1021/ol702056s⟩
Organic Letters, American Chemical Society, 2007, 9 (23), pp.4745-8. ⟨10.1021/ol702056s⟩
International audience; A stereoselective synthesis of heavily functionalized six-membered ring subunits, which possess functionality at sites appropriate for further elaboration, is described. The cyclopentanone moiety of hydrindenediol is required
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::030dc74e2afad92d3aff1156ecef43ad
https://hal.archives-ouvertes.fr/hal-00185594
https://hal.archives-ouvertes.fr/hal-00185594
Publikováno v:
Organic Letters; Nov2007, Vol. 9 Issue 23, p4745-4748, 4p