Zobrazeno 1 - 10
of 344
pro vyhledávání: '"Lukas J. Goossen"'
Autor:
Xianglin Luo, Peichao Hou, Jiayi Shen, Yifeng Kuang, Fengchao Sun, Huanfeng Jiang, Lukas J. Gooßen, Liangbin Huang
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-10 (2024)
Abstract Carboxylates are ideal directing groups because they are widely available, readily cleavable and excellent linchpins for diverse follow-up reactions. However, their use in meta-selective C−H functionalizations remains a substantial unmet c
Externí odkaz:
https://doaj.org/article/aca8bd4abc6f4508905d0d2644ba8e8b
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-8 (2020)
Since its discovery, the Hofer-Moest mechanism strongly limits the scope of electrochemical decarboxylative etherification. Here, the authors report the electrochemical conversion of carboxylic acids into alkyl benzotriazole ethers expanding the scop
Externí odkaz:
https://doaj.org/article/d177271950004c22b046a1091c8f4a54
Publikováno v:
HardwareX, Vol 10, Iss , Pp e00211- (2021)
Benchtop nuclear magnetic resonance (NMR) spectrometers are versatile analytic instruments with low acquisition and operation cost. However, in the basic version, samples must be manually measured one after the other. We herein describe the open-sour
Externí odkaz:
https://doaj.org/article/14aa8689082d48b7b7f0f563379066c4
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2737-2744 (2018)
A convenient and sustainable three-step synthesis of the tyrosinase inhibitor 2-hydroxy-6-tridecylbenzoic acid was developed that starts directly from the anacardic acid component of natural cashew nutshell liquid (CNSL). Natural CNSL contains 60–7
Externí odkaz:
https://doaj.org/article/5512d65bcfc0449c9ae0231414b3385b
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-7 (2016)
Amide formation is a ubiquitous reaction in organic chemistry, but suffers from the problem of generating large amounts of waste. Here, the authors report a catalytic amide synthesis by the ruthenium catalysed addition of carboxylic acids to acetylen
Externí odkaz:
https://doaj.org/article/68da9c19f6924ffc9968ed44e9e56cf5
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, p 43 (2010)
A new protocol for the decarboxylative Heck vinylation of benzoic acids is disclosed. In the presence of a catalyst system generated in situ from Pd(OAc)2 (2 mol %), CuF2 (2 equiv), and benzoquinone (0.5 equiv) in NMP, a wide range of olefins were co
Externí odkaz:
https://doaj.org/article/7af280a9c43a4768b025fd7dbf914b92
Publikováno v:
Handbook of CH‐Functionalization. :1-48
Autor:
Tim van Lingen, Valentina Bragoni, Marco Dyga, Benjamin Exner, Daniel Schick, Christoph Held, Gabriele Sadowski, Lukas J. Gooßen
Publikováno v:
Angewandte Chemie.
Autor:
Tim van Lingen, Valentina Bragoni, Marco Dyga, Benjamin Exner, Daniel Schick, Christoph Held, Gabriele Sadowski, Lukas J. Gooßen
Publikováno v:
Angewandte Chemie International Edition.
Publikováno v:
Angewandte Chemie International Edition.