Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ahmet Yesilcimen"'
Publikováno v:
Journal of the American Chemical Society. 144:6173-6179
Autor:
Masayuki Wasa, Ahmet Yesilcimen
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 79:1065-1072
Publikováno v:
J Am Chem Soc
We disclose a catalytic method for the enantio- and diastereo-selective union of alkyl ethers and hetero dienes. We demonstrate that a chiral Cu–BOX complex catalyzes the efficient oxidation of ethers into enol ethers in the presence of trityl acet
Publikováno v:
Organic & Biomolecular Chemistry. 18:7090-7093
We disclose a method for sequential Conia-ene-type cyclization/Negishi coupling for the union of alkynyl ketones and aryl iodides. This process is promoted through cooperative actions of Lewis acidic B(C6F5)3, ZnI2, Pd-based complex, and a Bronsted b
Publikováno v:
Journal of the American Chemical Society. 141:4199-4203
An efficient and highly enantioselective Conia-ene-type process has been developed. Reactions are catalyzed by a combination of B(C6F5)3, an N-alkylamine and a BOX–ZnI2 complex. Specifically, through cooperative action of B(C6F5)3 and amine, ketone
Publikováno v:
Org Biomol Chem
We disclose a method for sequential Conia-ene-type cyclization/Negishi coupling for the union of alkynyl ketones and aryl iodides. This process is promoted through cooperative actions of Lewis acidic B(C(6)F(5))(3), ZnI(2), Pd-based complex, and a Br
Publikováno v:
J Am Chem Soc
An efficient catalytic method to convert an α-C-H bond of N-alkylamines into an α-C-alkynyl bond was developed. In the past, such transformations were carried out under oxidative conditions, and the enantioselective variants were confined to tetrah
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b53d763a502435ae629e30ca549dbe51
https://europepmc.org/articles/PMC8048775/
https://europepmc.org/articles/PMC8048775/
Autor:
Min Cao, Bochao Zhang, Masayuki Wasa, Yejin Chang, Yuyang Zhang, Ahmet Yesilcimen, Jessica Z. Chan
Publikováno v:
Journal of the American Chemical Society. 141(37)
An efficient deuteration process of β-amino C─H bonds in various N-alkylamine-based pharmaceutical compounds has been developed. Catalytic reactions begin with the action of Lewis acidic B(C(6)F(5))(3) and Brønsted basic N-alkylamine, converting
Publikováno v:
Journal of the American Chemical Society. 141(10)
An efficient and highly enantioselective Conia-ene-type process has been developed. Reactions are catalyzed by a combination of B(C(6)F(5))(3), an N-alkylamine and a BOX–ZnI(2) complex. Specifically, through cooperative action of B(C(6)F(5))(3) and