Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Gong-Bin Huang"'
Publikováno v:
Organic Chemistry Frontiers. 10:1463-1469
A synergistic NHC/Ni catalyzed asymmetric reductive coupling of nitrobenzyl bromides with cyclic ketimines via SET process was realized.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a56b4f638113a5a1a86175bf14b078bc
https://doi.org/10.1039/d2qo01940j
https://doi.org/10.1039/d2qo01940j
Transition metal-free synthesis of α-aryl ketones via oxyallyl cation capture with arylboronic acids
Publikováno v:
Organic Chemistry Frontiers. 7:2480-2485
Herein, we describe a novel transition metal-free, umpolung strategy for the α-arylation of ketones by capturing transient oxyallyl cations with arylboronic acids. A variety of α-arylated ketones were obtained in moderate to good yields with broad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::127748aae83a14ec747bf94c025f4eec
https://doi.org/10.1039/d0qo00447b
https://doi.org/10.1039/d0qo00447b
Autor:
Jiang Weng, Dong‐Liang Xu, Gui Lu, Wei-Hua Huang, Xiu‐Hua Zheng, Pei‐Hong Zhai, Xiao‐Chen Qu, Gong-Bin Huang, Jing Guo
Publikováno v:
Advanced Synthesis & Catalysis. 361:1241-1246
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4e66dbf4b4e30575dbd3730288dcca0
https://doi.org/10.1002/adsc.201801446
https://doi.org/10.1002/adsc.201801446
Publikováno v:
Organic Chemistry Frontiers. 6:1955-1960
An efficient protocol for the synthesis of 1,1,2-triarylethanes and 2,2-diarylethylamine with biological and pharmacological potential via organo-photoredox-catalyzed decarboxylative 1,6-conjugate addition of carboxylic acids to para-quinone methides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ad73aad7d007007aaf851731e2737b3
https://doi.org/10.1039/c9qo00380k
https://doi.org/10.1039/c9qo00380k
Publikováno v:
Organicbiomolecular chemistry. 18(5)
An efficient protocol to access 2,2-diarylethylamines via visible-light-promoted radical reactions of para-quinone methides (p-QMs) with N-alkyl anilines has been disclosed. These reactions feature metal-free, redox-neutral, and mild reaction conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2092870131047aa8de6498b8c1e364a7
https://pubmed.ncbi.nlm.nih.gov/31956869
https://pubmed.ncbi.nlm.nih.gov/31956869
Publikováno v:
RSC Advances. 8:30946-30949
An efficient and general method of nucleophilic substitution of benzylic alcohols catalyzed by non-metallic Lewis acid B(C6F5)3 was developed. The reaction could be carried out under mild conditions and more than 35 examples of ethers, thioethers and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edfa7798d630de10c3115db35863ed57
https://doi.org/10.1039/c8ra05811c
https://doi.org/10.1039/c8ra05811c
Publikováno v:
Tetrahedron Letters. 57:5493-5496
3,3′-Bisindoles are known to be important structural motifs found in bioactive natural products, pharmaceuticals, and functional materials. Herein, a novel indoxyl-based approach was established for the synthesis of unsymmetrical 3,3′-biindoles f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41c3fd052200ec7534a6b935a02a9158
https://doi.org/10.1016/j.tetlet.2016.10.099
https://doi.org/10.1016/j.tetlet.2016.10.099
Publikováno v:
RSC advances. 8(54)
An efficient and general method of nucleophilic substitution of benzylic alcohols catalyzed by non-metallic Lewis acid B(C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c90435381c36434a1bf6bcf28edabfe8
https://pubmed.ncbi.nlm.nih.gov/35548750
https://pubmed.ncbi.nlm.nih.gov/35548750
Publikováno v:
ChemInform. 46
Using N′-aryl acylhydrazines as aryl donors, a novel copper(II)-catalyzed homo-coupling reaction of N′-aryl acylhydrazines has been developed for the synthesis of N′,N′-diaryl acylhydrazines. We also provided a complementary procedure for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9789f9183eb1d27513cfe11336775e8b
https://doi.org/10.1002/chin.201525103
https://doi.org/10.1002/chin.201525103
Autor:
Liang, Rui‐Xue1 (AUTHOR), Ma, Qi‐Yu1 (AUTHOR), Xiang, Tuan‐Xiu1 (AUTHOR), Zhang, You‐Ping1 (AUTHOR), Gong, Ya‐Nan1 (AUTHOR), Huang, Bin1 (AUTHOR), Wang, Bang‐Jin1 (AUTHOR), Xie, Sheng‐Ming1 (AUTHOR), Zhang, Jun‐Hui1 (AUTHOR) zjh19861202@126.com, Yuan, Li‐Ming1 (AUTHOR) yuan_limingpd@126.com
Publikováno v:
Journal of Separation Science. Sep2023, Vol. 46 Issue 18, p1-12. 12p.