Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Monica Quai"'
Publikováno v:
Tetrahedron Letters. 45:1413-1416
New insights into the cycloaddition reaction between alkyl isocyanides and benzyliden-1,3-diketones are reported. 5-Hydroxy-N-substituted-2H-pyrrol-2-ones and not substituted furans, as previously reported, are formed. The proof of the structure reli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6347f318fc3cafcac81d8a639a3fe87
https://doi.org/10.1016/j.tetlet.2003.12.059
https://doi.org/10.1016/j.tetlet.2003.12.059
Publikováno v:
Tetrahedron Letters. 42:6827-6829
The Wittig reaction of a pool of stabilised ylides and aromatic aldehydes was carried out in a microwave oven. Only a few minutes were needed for high conversion rates under microwave heating in comparison to hour time with traditional methods.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::585ba278f64c3b5c7773a5f380f786e5
https://doi.org/10.1016/s0040-4039(01)01384-3
https://doi.org/10.1016/s0040-4039(01)01384-3
Publikováno v:
Tetrahedron Letters. 42:4951-4953
[3+2] Cycloaddition of alkynes to resin bound nitrile oxides gives after cleavage of 3,4,5 trisubstituted isoxazoles in acceptable yields and fair to good purity, depending on the alkyne substituents. The reaction has been automated on the ACT 496 sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::927678efc08830cb92fa4adfbd255f37
https://doi.org/10.1016/s0040-4039(01)00904-2
https://doi.org/10.1016/s0040-4039(01)00904-2
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e648f0b1dd2aede2dc63b8cac9fe5a4e
https://doi.org/10.1002/chin.200152050
https://doi.org/10.1002/chin.200152050
Publikováno v:
ChemInform. 38
Phenoxy benzyl ethers are easily and quickly deprotected in the presence of ammonium formate and microencapsulated Pd(0)EnCat with the assistance of microwave irradiation. This procedure can be applied in the presence of other functional groups as we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5bd238a3cc628013fc94754196fdf49
https://doi.org/10.1002/chin.200721041
https://doi.org/10.1002/chin.200721041
Publikováno v:
ChemInform. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b8bc95de67eb66783419b43b54557f9
https://doi.org/10.1002/chin.200615254
https://doi.org/10.1002/chin.200615254