Site-selective modification of peptides using rhodium and palladium catalysis: complementary electrophilic and nucleophilic arylation

2007 ◽  
pp. 3903 ◽  
Author(s):  
Christopher J. Chapman ◽  
Ai Matsuno ◽  
Christopher G. Frost ◽  
Michael C. Willis

Author(s):  
Subhadip Maiti ◽  
Tirtha Mandal ◽  
Barada Prasanna Dash ◽  
Jyotirmayee Dash


2020 ◽  
Vol 6 (51) ◽  
pp. eabd1378
Author(s):  
Ben Dong ◽  
Jiasheng Qian ◽  
Mingjie Li ◽  
Zheng-Jun Wang ◽  
Minyan Wang ◽  
...  

The first development of an external oxidant-compatible system involving a phosphorus(III)-directed C–H functionalization has been uncovered. An efficient C–H esterification of indoles with CO and alcohols has been reported in which the high reactivity and the exclusive C7-selectivity derives from the selection of a P(III)–directing group and the utilization of benzoquinone as an external oxidant with palladium catalysis. This strategy shows many advantages, involving an easily accessible and removable directing group, the use of cheap carbonylation sources, a broad substrate scope, and excellent positional selectivity. Two cyclopalladated intermediates were confirmed by x-ray analysis, uncovering key mechanistic features of this P(III)-directed C–H metalation event.



2020 ◽  
Vol 11 (39) ◽  
pp. 10764-10769 ◽  
Author(s):  
Yu-Feng Liang ◽  
Long Yang ◽  
Becky Bongsuiru Jei ◽  
Rositha Kuniyil ◽  
Lutz Ackermann

B–H: site-selective B(3,4)–H arylations were accomplished at room temperature by versatile palladium catalysis enabled by weakly coordinating amides.



ChemInform ◽  
2008 ◽  
Vol 39 (7) ◽  
Author(s):  
Christopher J. Chapman ◽  
Ai Matsuno ◽  
Christopher G. Frost ◽  
Michael C. Willis


2011 ◽  
Vol 76 (3) ◽  
pp. 749-759 ◽  
Author(s):  
David Lapointe ◽  
Thomas Markiewicz ◽  
Christopher J. Whipp ◽  
Amy Toderian ◽  
Keith Fagnou


2016 ◽  
Vol 7 (4) ◽  
pp. 2804-2808 ◽  
Author(s):  
Yongbing Liu ◽  
Ke Yang ◽  
Haibo Ge

The direct coupling of unactivated sp3 C–H bonds in aliphatic amides with acetonitrile was achieved via palladium catalysis.



2019 ◽  
Vol 141 (25) ◽  
pp. 10048-10059 ◽  
Author(s):  
Jinwon Jeon ◽  
Ho Ryu ◽  
Changseok Lee ◽  
Dasol Cho ◽  
Mu-Hyun Baik ◽  
...  


2018 ◽  
Vol 140 (42) ◽  
pp. 13570-13574 ◽  
Author(s):  
William A. Golding ◽  
Robert Pearce-Higgins ◽  
Robert J. Phipps




1996 ◽  
Vol 451 ◽  
Author(s):  
D. Lincot ◽  
M. J. Furlong ◽  
M. Froment ◽  
R. Cortes ◽  
M. C. Bernard

ABSTRACTChalcogenide semiconductors have been deposited epitaxially from aqueous solutions either chemically or electrochemically at growth rates of up to 0.7 μmhr−1. After recalling the basic principles of these deposition processes, results are presented concerning chemically deposited CdS on InP, GaP and CuInSe2 substrates, electrodeposited CdTe on InP, and CdSAnP heterostructures. Characterisation of these structures by RHEED, TEM, HRTEM, and glazing angle X ray diffraction allows to analyse the effects of substrate orientation, polarity, lattice match plus the influence of temperature on epitaxial growth. These results are discussed in terms of self organisation and a site selective growth mechanisms due to the free enegy of formation of each compound.



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