Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Steve Tisserand"'
Publikováno v:
European Journal of Organic Chemistry. 2010:1869-1874
Nucleophilic mixed chromium(II) and chromium(III) acetylides are generated from the smooth reduction of primary 1,1,1-trichloroalkanes with chromium(II) chloride in the presence of an excess amount of triethylamine at room temperature. These species
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4ee3992241b519f05b43f6a34ba93bd
https://doi.org/10.1002/ejoc.200901476
https://doi.org/10.1002/ejoc.200901476
Publikováno v:
Tetrahedron Letters. 48:3855-3858
Using CrCl 2 in THF at room temperature, trichloromethyl carbinols and trichloromethylalkanes are readily transformed to the highly reactive α-chlorocarbenes, carbynes and α-chloro-α-chromium(III) vinylidene carbenoids. A mechanistic study is carr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd225edf99c60c9f275eecdc0bbe61b8
https://doi.org/10.1016/j.tetlet.2007.03.150
https://doi.org/10.1016/j.tetlet.2007.03.150
Publikováno v:
Tetrahedron Letters. 47:5177-5180
CrCl2-mediated condensation of γ-chloro-gem-trichloroalkanes with aldehyde generates homoallylic alcohols through a hydride rearrangement followed by a Nozaki–Hiyama allylation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fe40baf56789791dd998f2700329749
https://doi.org/10.1016/j.tetlet.2006.05.045
https://doi.org/10.1016/j.tetlet.2006.05.045
Publikováno v:
Tetrahedron Letters. 48:7117-7119
An efficient total synthesis of rhein and diacerhein has been accomplished by relying on a remarkable regioselective directed ortho metalation (DOM) followed by a one-pot two step addition-cyclization reaction, generating phthalide 5 intermediate eff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::650161713ad7bf5310d4542c1b76ccbd
https://doi.org/10.1016/j.tetlet.2007.07.218
https://doi.org/10.1016/j.tetlet.2007.07.218
Publikováno v:
Organic Letters. 7:2555-2557
[reaction: see text] Baylis-Hillman adducts were found to be excellent dienophiles in Diels-Alder reactions, providing essentially complete diastereocontrol (although mixtures of endo/exo isomers) with all dienes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdb1002ff90f973ffbf80d7b6fe02c96
https://doi.org/10.1021/ol050584f
https://doi.org/10.1021/ol050584f
Publikováno v:
ChemInform. 41
Nucleophilic mixed chromium(II) and chromium(III) acetylides are generated from the smooth reduction of primary 1,1,1-trichloroalkanes with chromium(II) chloride in the presence of an excess amount of triethylamine at room temperature. These species
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d210e323bc68c39974178153db54b10d
https://doi.org/10.1002/chin.201033062
https://doi.org/10.1002/chin.201033062
Autor:
Lik Ren Tai, Eddie L. Myers, Anders Palmelund, Varinder K. Aggarwal, Steve Tisserand, Craig P. Butts
Publikováno v:
ChemInform. 39
Dienes have been formed with good stereoselectivity and in good yield from simple aldehydes and acrylates/acrylonitrile in the presence of a phosphine and a Lewis acid through a modification of the Morita reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4af868a4ca6b26eb8e9ded3a220a1910
https://doi.org/10.1002/chin.200810057
https://doi.org/10.1002/chin.200810057
Autor:
Lik Ren Tai, Varinder K. Aggarwal, Anders Palmelund, Steve Tisserand, Eddie L. Myers, Craig P. Butts
Publikováno v:
Chemical communications (Cambridge, England). (40)
Dienes have been formed with good stereoselectivity and in good yield from simple aldehydes and acrylates/acrylonitrile in the presence of a phosphine and a Lewis acid through a modification of the Morita reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::198e9c920c02497f3e4c32882d95dde3
https://pubmed.ncbi.nlm.nih.gov/17925951
https://pubmed.ncbi.nlm.nih.gov/17925951
Publikováno v:
ChemInform. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aca18276849f362ebca5b14270d43c76
https://doi.org/10.1002/chin.200520226
https://doi.org/10.1002/chin.200520226
Publikováno v:
The Journal of Organic Chemistry. 69:8982-8983
Short and practical total syntheses of rhein (1) and diacerhein (2) have been achieved via a Fries rearrangement and bis-carbonylation strategy followed by cyclization in molten salt, starting from dibromoester 7.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a354407d63a1d915c4323606da0fb72
https://doi.org/10.1021/jo049228l
https://doi.org/10.1021/jo049228l