Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Miran Lemmerer"'
Publikováno v:
JACS Au, Vol 4, Iss 7, Pp 2456-2461 (2024)
Externí odkaz:
https://doaj.org/article/412ca1cd13c64e7aba4719eb29fb93d6
Publikováno v:
Molecules, Vol 24, Iss 17, p 3098 (2019)
A short approach to chiral diaza-olefines from protected 2,2′-diamino-1,1′-binaphthyl is presented. Cis- and trans-olefines can be selectively obtained by twofold N-allylation followed by RCM or by bridging a 2,2′-diamino-1,1′-binaphthyl prec
Externí odkaz:
https://doaj.org/article/5b219372dc8849b487d18272a7740b1d
Autor:
Miran Lemmerer
Publikováno v:
Organic Syntheses. 100:136-158
Publikováno v:
University of Vienna-u:cris
Autor:
Ján Matyasovsky, Nicolas Malzer, Nuno Maulide, Sebastian Heindl, Miran Lemmerer, Margaux Riomet
Publikováno v:
Angewandte Chemie. 133:19271-19275
Autor:
Miran Lemmerer, Haoqi Zhang, Anthony J. Fernandes, Tobias Fischer, Marianne Mießkes, Yi Xiao, Nuno Maulide
Publikováno v:
Angewandte Chemie International Edition. 61
Herein we report a method for the synthesis of α-aryl acrylamides leveraging polar S-to-C aryl migrations induced by a Lewis basic organocatalyst. In contrast to previously reported radical aryl migrations of sulfonyl acrylimides, this polar process
Autor:
Miran Lemmerer, Haoqi Zhang, Anthony J. Fernandes, Tobias Fischer, Marianne Mießkes, Yi Xiao, Nuno Maulide
Publikováno v:
Angewandte Chemie. 134
Autor:
Miran Lemmerer, Margaux Riomet, Ricardo Meyrelles, Boris Maryasin, Leticia González, Nuno Maulide
Publikováno v:
Angewandte Chemie. 134
Autor:
Nuno Maulide, Boris Maryasin, Margaux Riomet, Leticia González, Miran Lemmerer, Ricardo Meyrelles
Publikováno v:
Angewandte Chemie (International ed. in English). 61(11)
A direct C-C coupling process that merges Michael acceptors and Eschenmoser's salt is presented. Although reminiscent of the Morita-Baylis-Hillman reaction, this process requires no Lewis base catalyst. The underlying mechanism was unveiled by a comb
Autor:
Miran Lemmerer, Sebastian Heindl, Nicolas Malzer, Nuno Maulide, Ján Matyasovsky, Margaux Riomet
Publikováno v:
Angewandte Chemie (International Ed. in English)
A chemoselective and robust protocol for the γ‐oxidation of β,γ‐unsaturated amides is reported. In this method, electrophilic amide activation, in a rare application to unsaturated amides, enables a regioselective reaction with TEMPO resulting