Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Regis Tripoli"'
Publikováno v:
Tetrahedron Letters. 40:4037-4040
Less highly substituted silyl enol ethers are regiospecifically prepared in high yield, around room temperature under kinetic conditions, from unsymmetrical cyclic ketones and magnesium bis(diisopropylamide) [(DA) 2 Mg] in THF/heptane. This high regi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d39b031c705f0853c036ffc5826def0b
https://doi.org/10.1016/s0040-4039(99)00665-6
https://doi.org/10.1016/s0040-4039(99)00665-6
Publikováno v:
ChemInform. 30
Less highly substituted silyl enol ethers are regiospecifically prepared in high yield, around room temperature under kinetic conditions, from unsymmetrical cyclic ketones and magnesium bis(diisopropylamide) [(DA) 2 Mg] in THF/heptane. This high regi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba091b7f7b4474e17ea4141427792969
https://doi.org/10.1002/chin.199932060
https://doi.org/10.1002/chin.199932060
Publikováno v:
Organicbiomolecular chemistry. 5(16)
Intramolecular Diels-Alder reactions of ester-linked 1,3,8-nonatrienes carrying a diphenylcyclopropyl substituent attached to C1 proceed with high levels of stereoselectivity. The stereochemical outcomes of these reactions are explained by reference
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62f19411570e3430a1d9efa67091322a
https://pubmed.ncbi.nlm.nih.gov/18019536
https://pubmed.ncbi.nlm.nih.gov/18019536
Publikováno v:
ChemInform. 37
Aldehydes are prepared in excellent yield by Wittig reactions of phosphoranes on the Weinreb amide of formic acid followed by in situ hydrolysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fd6fe902aab71fbe7bb0c5f1c8a9ad8
https://doi.org/10.1002/chin.200648064
https://doi.org/10.1002/chin.200648064
Publikováno v:
ChemInform. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca754c769b4f2e743769fdb8ce1411e
https://doi.org/10.1002/chin.200548200
https://doi.org/10.1002/chin.200548200