共查询到20条相似文献,搜索用时 15 毫秒
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Sarah E. Walker James A. Jordan‐Hore David G. Johnson Stuart A. Macgregor Ai‐Lan Lee 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(50):14096-14099
A direct Pd‐catalyzed C H functionalization of benzoquinone (BQ) can be controlled to give either mono‐ or disubstituted BQ, including the installation of two different groups in a one‐pot procedure. BQ can now be directly functionalized with aryl, heteroaryl, cycloalkyl, and cycloalkene groups and, moreover, the reaction is conducted in environmentally benign water or acetone as solvents. 相似文献
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Jimin Xu Guolin Cheng Deyong Su Yantao Liu Xinyan Wang Yuefei Hu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(47):13105-13110
A novel palladium catalyzed direct ortho‐arylation of N‐phenacylpyridinium bromide was developed. The amazing N‐phenacyl group regioselectively activates the C? H bond of pyridine and automatically departs from the arylated products. A kinetic isotope effect study proved that the reaction went through a C? H‐bond activation pathway and 2,6‐diphenylpyridine was produced stepwise from 2‐phenylpyridine. 相似文献
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Masashi Shigenobu Kazuhiro Takenaka Hiroaki Sasai 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2015,127(33):9708-9712
A palladium‐catalyzed direct arylation of isoxazoles with aryl iodides has been achieved. The C H bond at the 5‐position is activated selectively to give coupling products in moderate to good yields. This direct arylation was applied to the synthesis of a spiro‐type chiral ligand, which proved to be most effective to the palladium‐catalyzed tandem cyclization of a dialkenyl alcohol. 相似文献
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Masashi Shigenobu Kazuhiro Takenaka Hiroaki Sasai 《Angewandte Chemie (International ed. in English)》2015,54(33):9572-9576
A palladium‐catalyzed direct arylation of isoxazoles with aryl iodides has been achieved. The C H bond at the 5‐position is activated selectively to give coupling products in moderate to good yields. This direct arylation was applied to the synthesis of a spiro‐type chiral ligand, which proved to be most effective to the palladium‐catalyzed tandem cyclization of a dialkenyl alcohol. 相似文献
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Zi‐Qi Lin Wei‐Zhen Wang Shao‐Bai Yan Wei‐Liang Duan 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2015,127(21):6363-6367
A palladium‐catalyzed enantioselective C H arylation of N‐(o‐bromoaryl)‐diarylphosphinic amides is described for the synthesis of phosphorus compounds bearing a P‐stereogenic center. The method provides good enantioselectivities and high yields. The products were readily transformed into P‐chiral biphenyl monophosphine ligands. 相似文献
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Prof. Dr. Hiroaki Ohno Mutsumi Iuchi Dr. Naoto Kojima Prof. Dr. Takehiko Yoshimitsu Prof. Dr. Nobutaka Fujii Prof. Dr. Tetsuaki Tanaka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(17):5352-5360
Palladium‐catalyzed cascade C? H alkenylation and arylation provides convenient access to polycyclic aromatic compounds. Treatment of 3‐bromoaniline derivatives bearing a bromocinnamyl group on the nitrogen atom with a catalytic amount of [Pd(OAc)2] and PCy3?HBF4 in the presence of Cs2CO3 in dioxane affords naphthalene‐fused indole derivatives in good yields. This double cyclization reaction is also applicable to heterocyclic substrates, giving fused indoles containing a heteroaromatic ring such as dibenzofuran, dibenzothiophene, carbazole, indole, or benzofuran through heterocyclic C? H arylation. When using a 2,6‐unsubstituted aniline derivative, the first C? H arylation preferentially proceeds at the more hindered position of the aniline ring. 相似文献
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Hai Zhou Yun‐He Xu Wan‐Jun Chung Teck‐Peng Loh Prof. 《Angewandte Chemie (International ed. in English)》2009,48(29):5355-5357
It does get in! A fluoride‐assisted direct cross‐coupling of cyclic enamides with trialkoxy aryl silanes by a palladium‐catalyzed C? H activation leads to a wide range of enamides in yields of up to 95 %.
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Yong‐Jun Bian Chao‐Yue Chen Prof. Zhi‐Zhen Huang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(3):1129-1133
An efficient palladium‐catalyzed C? H functionalization of aldehydes with various N‐substituted N‐heteroarene‐2‐carboxamides has been developed for the synthesis of secondary imides. The reaction tolerates various functionalities, such as methoxy, fluoro, chloro, and bromo groups. A tentative radical mechanism for a PdII/PdIV catalytic cycle is proposed. 相似文献
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Upendra Sharma Rajesh Kancherla Togati Naveen Soumitra Agasti Debabrata Maiti 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(44):12089-12093
A palladium‐catalyzed dehydrogenative coupling between diarylamines and olefins has been discovered for the synthesis of substituted indoles. This intermolecular annulation approach incorporates readily available olefins for the first time and obviates the need of any additional directing group. An ortho palladation, olefin coordination, and β‐migratory insertion sequence has been proposed for the generation of olefinated intermediate, which is found to produce the expected indole moiety. 相似文献
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Lutz Ackermann Prof. Dr. Rubén Vicente Dr. Anant R. Kapdi Dr. 《Angewandte Chemie (International ed. in English)》2009,48(52):9792-9826
The area of transition‐metal‐catalyzed direct arylation through cleavage of C? H bonds has undergone rapid development in recent years, and is becoming an increasingly viable alternative to traditional cross‐coupling reactions with organometallic reagents. In particular, palladium and ruthenium catalysts have been described that enable the direct arylation of (hetero)arenes with challenging coupling partners—including electrophilic aryl chlorides and tosylates as well as simple arenes in cross‐dehydrogenative arylations. Furthermore, less expensive copper, iron, and nickel complexes were recently shown to be effective for economically attractive direct arylations. 相似文献
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