Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Bing-Tao Ren"'
Publikováno v:
Organic Chemistry Frontiers. 9:3956-3960
An asymmetric IEDDA reaction of 2-pyrones with indenes catalyzed by a chiral N,N′-dioxide/Ni(OTf)2 complex has been disclosed to construct highly functionalized hexahydrofluorenyl bridged-lactone scaffolds in high yields and ee.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d7eb0fc5457f87acce699eb15167260
https://doi.org/10.1039/d2qo00493c
https://doi.org/10.1039/d2qo00493c
Publikováno v:
Chemical Science. 13:5562-5567
An enantioselective IEDDA reaction between 2-pyrone and cyclic enamine was realized to construct cis-hydroindoles in high yield and ee, providing a concise route for formal total synthesis of (+)-minovincine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecd3d168ff24171bf593b94a74ac1bfa
https://doi.org/10.1039/d2sc01458k
https://doi.org/10.1039/d2sc01458k
Autor:
Ying-yi Hu, Rui-hua Zhong, Xiang-jie Guo, Guo-ting Li, Jie-yun Zhou, Wen-jie Yang, Bing-tao Ren, Yan Zhu
Publikováno v:
Journal of Ethnopharmacology. 307:116242
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5afa5ecd169847541372595509b8312e
https://doi.org/10.1016/j.jep.2023.116242
https://doi.org/10.1016/j.jep.2023.116242
Publikováno v:
Chemical science. 13(19)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::380a46201f5da621a2b357f6a16ab329
https://pubmed.ncbi.nlm.nih.gov/35694337
https://pubmed.ncbi.nlm.nih.gov/35694337
Autor:
Yan-Le Mei, Jing Xue, Fang-Shuai Zhou, Guang-Yi Zhang, Wei Zhou, Qing-Hai Deng, Tao Huo, Cheng Zhong, Bing-Tao Ren
Publikováno v:
Organic Letters. 21:9598-9602
An efficient rhodium-catalyzed redox-neutral annulations of N-phenoxyacetamides and ynones via successive double C–H bond activations has been developed. A series of novel and complex indenols bearing a benzofuran unit were generated with moderate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bab74cf281df7fb87644f14767e0f73
https://doi.org/10.1021/acs.orglett.9b03766
https://doi.org/10.1021/acs.orglett.9b03766
Publikováno v:
The Journal of Organic Chemistry. 84:6557-6564
The efficient and practical nucleophilic cyanation and trifluoromethylation with appropriate trimethylsilyl nucleophiles were developed. Catalytic amounts of cheap and nontoxic Cs2CO3 were used to ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55aa7f4c6ee29aa19ee35c071a4753a6
https://doi.org/10.1021/acs.joc.9b00999
https://doi.org/10.1021/acs.joc.9b00999
Autor:
Hubert Wadepohl, David Bürgy, Yan-Kai Liu, Lutz H. Gade, Qing-Hai Deng, Bin Li, Clemens K. Blasius, Ina Michalsky, Bing-Tao Ren
Publikováno v:
The Journal of organic chemistry. 85(10)
Two synthetic strategies for a new family of neutral NON ligands featuring a "bis(oxazolinylmethylidene)isobenzofuran" framework (boxman) are reported. A Pd-mediated cyclization reaction forming the isobenzofuran core constitutes the key reaction in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ddef89751a02d61959cb711fa0ee042
https://pubmed.ncbi.nlm.nih.gov/32286820
https://pubmed.ncbi.nlm.nih.gov/32286820
Autor:
Qing-Hai Deng, Bing-Tao Ren, Guang-Yi Zhang, Wei Zhou, Chong-Ji Wang, Jing Xue, Jian Sun, Yan-Le Mei
Publikováno v:
Organic letters. 21(18)
The first example of copper-catalyzed enantioselective dearomative azidation of β-naphthols using a readily available N3-transfer reagent is reported. A series of 2-hydroxy-1-naphthamides bearing a complex N-substituent were converted to the corresp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf50302ae182cc9de08b0a0f70aec58e
https://pubmed.ncbi.nlm.nih.gov/31475534
https://pubmed.ncbi.nlm.nih.gov/31475534
Autor:
Ling-Feng, Jiang, Bing-Tao, Ren, Bin, Li, Guang-Yi, Zhang, Yi, Peng, Zhen-Yu, Guan, Qing-Hai, Deng
Publikováno v:
The Journal of organic chemistry. 84(11)
The efficient and practical nucleophilic cyanation and trifluoromethylation with appropriate trimethylsilyl nucleophiles were developed. Catalytic amounts of cheap and nontoxic Cs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5e051da643499e7fe2e281456996c06f
https://pubmed.ncbi.nlm.nih.gov/31090405
https://pubmed.ncbi.nlm.nih.gov/31090405
Publikováno v:
Organic Letters; Sep2019, Vol. 21 Issue 18, p7315-7319, 5p