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of 5
pro vyhledávání: '"Benedikt Nissl"'
Autor:
Yuta Hioki, Matteo Costantini, Jeremy Griffin, Kaid C. Harper, Melania Prado Merini, Benedikt Nissl, Yu Kawamata, Phil S. Baran
Publikováno v:
Science. 380:81-87
The Kolbe reaction forms carbon-carbon bonds through electrochemical decarboxylative coupling. Despite more than a century of study, the reaction has seen limited applications owing to extremely poor chemoselectivity and reliance on precious metal el
Autor:
Yuta Hioki, Matteo Costantini, Jeremy Griffin, Kaid Harper, Melania Prado Merini, Benedikt Nissl, Yu Kawamata, Phil Baran
The Kolbe reaction has seen limited applications owing to its extremely poor chemoselectivity and reliance on precious metal-based electrodes, despite its potential to be one of the workhorse reactions of organic synthesis for C–C bond formation in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b36a558d7327e089b5f9814633d7f9c7
https://doi.org/10.26434/chemrxiv-2022-3cj82-v2
https://doi.org/10.26434/chemrxiv-2022-3cj82-v2
Autor:
Florian Trauner, Felix Reiners, Kodjo-Edmond Apaloo-Messan, Benedikt Nißl, Muhammad Shahbaz, Dongfang Jiang, Julian Aicher, Dorian Didier
Publikováno v:
Chemical communications (Cambridge, England). 58(15)
The addition of nucleophilic organometallic species onto in situ generated azabicyclobutanes enables the selective formation of 3-arylated azetidine intermediates through strain-release. Single pot strategies were further developed for the N-arylatio
Publikováno v:
Organic Letters. 22:8533-8537
Non-natural azetidine-based amino acids (Aze) present interesting features in protein engineering. A simple organometallic route toward unsaturated carboxylic acid precursors is presented. Subsequent metal-catalyzed asymmetric reduction allowed for t
Recent progress on four-membered ring building blocks has led us to investigate the formation of non-natural azetidine-based amino acids (Aze). A simple organometallic route was developed to access unsaturated carboxylic acids, which were further eng
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf53c71b946649fc2bbc90358082d097
https://doi.org/10.26434/chemrxiv.12966803
https://doi.org/10.26434/chemrxiv.12966803