Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Arne Heusler"'
Publikováno v:
Angewandte Chemie (International Ed. in English)
Angewandte Chemie International Edition
Angewandte Chemie International Edition
Dearomatization is an effective method to transform readily available N‐heterocycles into partially saturated motifs. Manipulation of dihydro‐derivatives holds great potential and provides access to a variety of semi‐saturated N‐heterocyclic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c0ed0f8343ebb502c17caa5dcf4f863
https://doi.org/10.1002/anie.202104115
https://doi.org/10.1002/anie.202104115
Publikováno v:
Angewandte Chemie. 133:13912-13916
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd10d9393b92e7271bc6f4856a890c8b
https://doi.org/10.1002/ange.202104115
https://doi.org/10.1002/ange.202104115
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry – A European Journal
Chemistry – A European Journal
Transfer hydrogenation reactions are of great interest to reduce diverse molecules under mild reaction conditions. To date, this type of reaction has only been successfully applied to alkenes, alkynes and polarized unsaturated compounds such as keton
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e3e595bf0b35130913b195f1e8898c0
https://doi.org/10.1002/chem.202002777
https://doi.org/10.1002/chem.202002777
Autor:
Tobias Wagener, Arne Heusler, Klaus Bergander, Constantin G. Daniliuc, Zackaria Nairoukh, Frank Glorius
Publikováno v:
ACS Catalysis
Fluorinated piperidines are desirable motifs for pharmaceutical and agrochemical research. Nevertheless, general synthetic access remains out of reach. Herein, we describe a simple and robust cis-selective hydrogenation of abundant and cheap fluoropy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b79d525335c443d54cb696b5bddeae33
https://doi.org/10.1021/acscatal.0c03278
https://doi.org/10.1021/acscatal.0c03278
Publikováno v:
Chemistry – An Asian Journal. 14:2656-2661
Herein, we report the conjugate addition of α,β-unsaturated carbonyl compounds to thiophene derivatives. We used a 2-iodoimidazolinium triflate salt as a halogen-bonding donor, which afforded moderate-to-excellent yields of the corresponding alkyla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbe3241b562dc03a9b05109f10bca898
https://doi.org/10.1002/asia.201900607
https://doi.org/10.1002/asia.201900607
Autor:
Xiaolong Zhang, Felix Schäfer, Kendall N. Houk, Shuming Chen, Arne Heusler, Renyu Guo, Jiajia Ma, M. Kevin Brown, Constantin G. Daniliuc, Peter Bellotti, Frank Glorius
Publikováno v:
Science (New York, N.Y.), vol 371, iss 6536
Science
Science
Heteroaromatics lured into cycloadditions The Diels-Alder reaction is widely used to produce six-membered carbon rings from alkenes and dienes. Heteroaromatics such as quinolines resemble dienes in principle, but in practice their pairs of double bon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf371a8da96160a982ec817e23206c72
https://escholarship.org/uc/item/4b48g1ss
https://escholarship.org/uc/item/4b48g1ss
Autor:
Lückemeier, Lukas, Heusler, Arne
Publikováno v:
Nachrichten aus der Chemie; Dec2023, Vol. 71 Issue 12, p87-87, 1p
Publikováno v:
ACS Catalysis
A trans-selective arene hydrogenation of abundant phenol derivatives catalyzed by a commercially available heterogeneous palladium catalyst is reported. The described method tolerates a variety of functional groups and provides access to a broad scop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3387532f96fbd58a15b23ed9d1b88043
Publikováno v:
Advanced Synthesis & Catalysis. 364(19):3366-3371
Saturated N-heterocycles are prominent motifs found in various natural products and pharmaceuticals. Despite the increasing interest in this class of compounds, the synthesis of saturated bicyclic azacycles requires tedious multi-step syntheses. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e030e7528ab79ab6f758413cca9b76f
Autor:
Wagener, Tobias1 (AUTHOR), Pierau, Marco1 (AUTHOR), Heusler, Arne1 (AUTHOR), Glorius, Frank1 (AUTHOR) glorius@uni-muenster.de
Publikováno v:
Advanced Synthesis & Catalysis. 10/4/2022, Vol. 364 Issue 19, p3366-3371. 6p.