Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Phillip Biallas"'
Publikováno v:
Organic letters. 24(10)
An iridium-catalyzed, reductive alkylation of abundant tertiary lactams and amides using 1-2 mol % of Vaska's complex (IrCl(CO)(PPh3)2), tetramethyldisiloxane (TMDS), and difluoro-Reformatsky reagents (BrZnCF2R) for the general synthesis of medicinal
Publikováno v:
European Journal of Organic Chemistry. 2020:4389-4398
Publikováno v:
The Journal of Organic Chemistry. 84:1654-1663
Diazidated malonamides derived from amines and diazidated diethyl malonate react with lithiated alcohols through nucleophilic substitution reactions where azide acts as an unconventional leaving group. This deazidoalkoxylation leads to the formal con
Publikováno v:
Polymer Chemistry. 10:60-64
A diazidated malonate derivative was employed as a monomer for the reagent-free one-pot synthesis of several polyamides containing geminal diazido moieties within the polymer backbone. Using different diamines, azide-rich polyamides with diverse prop
Publikováno v:
European Journal of Organic Chemistry. 2017:1526-1539
We have discovered that 2,2-diazido acylacetates, a class of compounds with essentially unknown reactivity, can be coupled to amines through a new strategy that does not involve any reagents. 2,2-Diazido acetate is the unconventional leaving group un
Autor:
Phillip Biallas, Stefan F. Kirsch
Publikováno v:
Tetrahedron Letters. 58:4209-4211
The complete hydrogenolysis of compounds containing the geminal diazido functionality is described. Using hydrogen over palladium on charcoal, the diazides are reduced, and primary amines are obtained. For example, aminomalonates and glycines are gen
Publikováno v:
Organicbiomolecular chemistry. 15(15)
A mild and convenient protocol for the oxidative cleavage of 1,3-diketone compounds is described. Under metal-free conditions, the method converts the 1,3-dicarbonyls into amides when treated with (nBu4N)N3 and iodine in the presence of an amine at r
Autor:
Andreas P. Haering, Phillip Biallas, Stefan F. Kirsch, Markus Roggel, My Linh Tong, Martin Juebermann, Fabian Mohr, Hellmuth Erhardt, Andreas Kotthaus
Publikováno v:
ChemInform. 47
Autor:
Fabian Mohr, My Linh Tong, Phillip Biallas, Martin Jübermann, Stefan F. Kirsch, Andreas Kotthaus, Andreas P. Häring, Hellmuth Erhardt, Markus Roggel
Publikováno v:
The Journal of organic chemistry. 80(24)
Geminal diazides constitute a rare class of compounds where only a limited number of methods are available for their synthesis. We present the reaction of 1,3-dicarbonyl compounds (as exemplified by malonates, 3-oxoesters, and 1,3-diketones) with mol
Autor:
'Phillip Biallas
Publikováno v:
Ken Yamazaki