Selective C-H Olefination of Indolines (C5) and Tetrahydroquinolines (C6) by Pd/S,O-Ligand Catalysis

Autor: Matthijs Hakkennes, Kit Ming Wong, Wen-Liang Jia, Kananat Naksomboon, Thomas Morsch, Nick Westerveld, M. Ángeles Fernández-Ibáñez

Publikováno v: Organic Letters, 21(23), 9339-9342. American Chemical Society
Organic Letters

Herein, we report a highly selective C-H olefination of directing-group-free indolines (C5) and tetrahydroquinolines (C6) by Pd/S,O-ligand catalysis. In the presence of the S,O-ligand, a wide range of challenging indolines, tetrahydroquinolines, and

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https://dare.uva.nl/personal/pure/en/publications/selective-ch-olefination-of-indolines-c5-and-tetrahydroquinolines-c6-by-pdsoligand-catalysis(06b9a089-c7e2-4b3b-a73c-b74157113cd0).html

Facile Synthesis of Pure 1,6,7,12-Tetrachloroperylene-3,4,9,10-tetracarboxy Bisanhydride and Bisimide

Autor: Ferdinand C. Grozema, Nick Westerveld, Rajeev K. Dubey, Ernst J. R. Sudhölter, Wolter F. Jager

Publikováno v: Organic Letters, 17(8), 1882-1885
Organic Letters 17 (2015) 8

A robust and scalable procedure to obtain pure 1,6,7,12-tetrachloroperylene-3,4,9,10-tetracarboxy bisanhydride, a highly valuable synthon, has been developed via synthesis of a novel intermediate compound 1,6,7,12-perylene-3,4,9,10-tetracarboxy tetra

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https://doi.org/10.1021/acs.orglett.5b00562

Substitution Effects on the Photoinduced Charge-Transfer Properties of Novel Perylene-3,4,9,10-tetracarboxylic Acid Derivatives

Autor: Wolter F. Jager, Jorrit Bleeker, Ferdinand C. Grozema, Nick Westerveld, Damla Inan, Rajeev K. Dubey

Publikováno v: The Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory, 121(24)
The Journal of Physical Chemistry A
The Journal of Physical Chemistry. a

We report here the synthesis and photophysical study of a series of electron donor–acceptor molecules, in which electron-donating 4-methoxyphenoxy groups are attached to the 1,7-bay positions of four different perylene tetracarboxylic acid derivati

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http://resolver.tudelft.nl/uuid:6d707ad8-faa0-4fba-9661-e06dabcbd8ff

Fluorescent PET probes based on perylene-3,4,9,10-tetracarboxylic tetraesters

Autor: Nick Westerveld, Rajeev K. Dubey, Wolter F. Jager, Gergely Knorr

Publikováno v: Organicbiomolecular chemistry. 14(5)

Perylene-3,4,9,10-tetracarboxylic tetraester-based fluorescent PET probes with aniline receptors attached either at the peri- or the bay-positions have been synthesized. By attaching aniline receptors at the bay position, pH-sensitive "light-up" prob

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46cf626d9ce9f781b97db0499e1b4440
https://pubmed.ncbi.nlm.nih.gov/26740333