多功能氧酰胺导向基在碳氢键活化反应中的研究进展

doi:10.3866/PKU.WHXB201812016

物理化学学报 >> 2019, Vol. 35 >> Issue (9): 989-1004.doi: 10.3866/PKU.WHXB201812016

所属专题：碳氢键活化

多功能氧酰胺导向基在碳氢键活化反应中的研究进展

朱月路¹,赵鑫阳¹,吴谦²,陈颖²,赵劲^1,*()

¹ 配位化学国家重点实验室，化学和生物医学科学研究所，南京大学化学与化工学院，南京 210093
² 广东省纳米材料研究重点实验室，北京大学深圳研究生院化学生物学与生物技术学院，广东深圳 518055

收稿日期:2018-12-05 录用日期:2019-01-15 发布日期:2019-01-21
通讯作者: 赵劲 E-mail:jingzhao@nju.edu.cn
作者简介:赵劲，出生于1978年。2005年获得美国耶鲁大学博士学位，随后赴加州大学伯克利分校和芝加哥大学进行博士后研究。2007年–2008年在美国罗门哈斯公司担任高级研究员。2008年–2014年南京大学生命科学学院教授。2014年起任南京大学化学化工学院教授。主要从事金属蛋白和金属酶的结构、生物相容的金属催化反应和荧光小分子探针的研究
基金资助:
国家自然科学基金(21622103);国家自然科学基金(21571098);国家自然科学基金(91753121);江苏省自然科学基金(BK20160022);深圳基础研究项目(JCYJ20170413150538897);中央大学基础研究经费(020514380139)

Research Advances in C―H Bond Activation of Multitasking N-Phenoxyamides

Yuelu ZHU¹,Xinyang ZHAO¹,Qian WU²,Ying CHEN²,Jing ZHAO^1,*()

¹ State Key Laboratory of Coordination Chemistry, Institute of Chemistry and BioMedical Sciences, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, P. R. China
² Guangdong Key Lab of Nano-Micro Material Research, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen 518055, Guangdong Province, P. R. China

Received:2018-12-05 Accepted:2019-01-15 Published:2019-01-21
Contact: Jing ZHAO E-mail:jingzhao@nju.edu.cn
Supported by:
the National Science Foundation of China(21622103);the National Science Foundation of China(21571098);the National Science Foundation of China(91753121);Natural Science Foundation of Jiangsu Province, China(BK20160022);Shenzhen Basic Research Program, China(JCYJ20170413150538897);Fundamental Research Funds for the Central Universities, China(020514380139)

摘要/Abstract

摘要：

近年来，通过导向基团进行碳氢键活化构建C―C键及C―X键的方法得到了快速发展，已成为有机合成的重要手段之一。在碳氢键活化中，作为多功能导向基团之一的氧酰胺，由于其独特的性质，引起了科学家们的广泛关注。氧酰胺中O―N键的氧化性替代外部氧化剂，使反应处于氧化还原中性。加入化学计量的外部氧化剂，通常可以使O―N键得到保留。在不同的溶剂中，能够表现出不同的区域选择性和立体选择性；皆体现了氧酰胺作为导向基团的独特之处。本文综述了N-苯氧基酰胺作为底物进行碳氢键活化的研究进展，同时根据现有的实验和理论研究结果对不同反应的机理进行了探讨。

关键词: 碳氢键活化, N-苯氧基酰胺, 多功能, 苯酚, 硒

Abstract:

Transition-metal-catalyzed C―H functionalization reactions, assisted by directing groups (DGs), have become some of the most powerful strategies to form C―C and C―X (X = O, N, S, etc.) bonds. It has brought about a revolution in the synthesis of drugs and natural products, and the method is widely applicable in the fields of material chemistry and pharmaceutical industry. This strategy has mainly focused on regioselective C―H functionalization of amides, esters, carbamates, and enamides with DGs to form C―C and C―X bonds. Since these DGs are relatively stable, they must be removed by other methods when the reaction is completed. Therefore, the use of a traceless DG is one of the important challenges for transition-metal-catalyzed C―H functionalization. Recently, N-phenoxyamide has been attracting significant research attention as a versatile DG. Oxyacetamide (O―NHAc) is one of the most versatile functionalities for directed C―H functionalization cascades, such as the internal oxidation with N―O bond cleavage. The O―NHAc has been reported as a superb DG for redox-neutral C―H activation/annulation cascade reactions to synthesize phenol and complex heterocyclic scaffolds by coupling with alkynes, alkenes, heteroarenes, and diazo compounds. However, for the external oxidation with preservation of the N―O bond, e.g. when a stoichiometric external oxidant is present, N-phenoxyamides could react with aldehydes or α, β-unsaturated aldehydes. In addition, the solvent can control the chemoselectivity. In this minireview, the C―H bond functionalization of N-phenoxyamide is divided into five categories according to the different substrates, viz. alkenes, alkynes, diazo, and other compounds and intramolecular C―H bond activation reactions. Based on experimental and theoretical research results, the reaction mechanism was discussed. In the first part, we summarize the ortho-alkylation, alkenylation, and cyclization of N-phenoxyamide with olefins. In the second part, we present the Rh- and Ir-catalyzed C―H activation or cyclization of N-phenoxyamide with alkanes to synthesize phenol or benzofuran compounds. In the third part, we describe the synthesis of phenolic compounds functionalized by Rh-catalyzed diazo compounds by carbene intermediates and N-phenoxyamides. The forth part summarizes the C―H activation/annulation reaction using aldehydes, heterocyclic aromatic, and sulfur reagents as substrates. The last part of the paper generalizes the intramolecular ortho-hydroxylation and ortho, para-amidation reactions.

Key words: C―H activation, N-phenoxyamides, Multitasking, Phenols, Selenium

朱月路,赵鑫阳,吴谦,陈颖,赵劲. 多功能氧酰胺导向基在碳氢键活化反应中的研究进展[J]. 物理化学学报, 2019, 35(9), 989-1004. doi: 10.3866/PKU.WHXB201812016

Yuelu ZHU,Xinyang ZHAO,Qian WU,Ying CHEN,Jing ZHAO. Research Advances in C―H Bond Activation of Multitasking N-Phenoxyamides[J]. Acta Physico-Chimica Sinica 2019, 35(9), 989-1004. doi: 10.3866/PKU.WHXB201812016

链接本文: https://www.whxb.pku.edu.cn/CN/10.3866/PKU.WHXB201812016

https://www.whxb.pku.edu.cn/CN/Y2019/V35/I9/989

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参考文献 77

1	Gutekunst W. R. ; Baran P. S. Chem. Soc. Rev. 2011, 40, 1976. doi: 10.1039/C0CS00182A
2	Wencel-Delord J. ; Droge T. ; Liu F. ; Glorius F. Chem. Soc. Rev. 2011, 40, 4740. doi: 10.1039/C1CS15083A
3	Arockiam P. B. ; Bruneau C. ; Dixneuf P. H. Chem. Rev. 2012, 112, 5879. doi: 10.1021/cr300153j
4	Li B. J. ; Shi Z. J. Chem. Soc. Rev. 2012, 41, 5588. doi: 10.1039/C2CS35096C
5	Liu C. ; Yuan J. ; Gao M. ; Tang S. ; Li W. ; Shi R. ; Lei A. Chem. Rev. 2015, 115, 12138. doi: 10.1021/cr500431s
6	He J. ; Wasa M. ; Chan K. S. L. ; Shao Q. ; Yu J. Q. Chem. Rev. 2017, 117, 8754. doi: 10.1021/acs.chemrev.6b00622
7	Park Y. ; Kim Y. ; Chang S. Chem. Rev. 2017, 117, 9247. doi: 10.1021/acs.chemrev.6b00644
8	Yi H. ; Zhang G. ; Wang H. ; Huang Z. ; Wang J. ; Singh A. K. ; Lei A. Chem. Rev. 2017, 117, 9016. doi: 10.1021/acs.chemrev.6b00620
9	Guo X. X. ; Gu D. W. ; Wu Z. ; Zhang W. Chem. Rev. 2015, 115, 1622. doi: 10.1021/cr500410y
10	Liu J. ; Chen G. ; Tan Z. Adv. Synth. Catal. 2016, 358, 1174. doi: 10.1002/adsc.201600031
11	Wendlandt A. E. ; Suess A. M. ; Stahl S. S. Angew. Chem. Int. Edit. 2011, 50, 11062. doi: 10.1002/anie.201103945
12	Abrams D. J. ; Provencher P. A. ; Sorensen E. J. Chem. Soc. Rev. 2018, 47, 8925. doi: 10.1039/c8cs00716k
13	Jayakumar J. ; Parthasarathy K. ; Chen Y. H. ; Lee T. H. ; Chuang S. C. ; Cheng C. H. Angew. Chem. Int. Edit. 2014, 53, 9889. doi: 10.1002/anie.201405183
14	Shan G. ; Flegel J. ; Li H. ; Merten C. ; Ziegler S. ; Antonchick A. P. ; Waldmann H. Angew. Chem. Int. Edit. 2018, 57, 14250. doi: 10.1002/anie.201809680
15	Yang W. ; Dong J. ; Wang J. ; Xu X. Org. Lett. 2017, 19, 616. doi: 10.1021/acs.orglett.6b03777
16	Wu J. Q. ; Zhang S. S. ; Gao H. ; Qi Z. ; Zhou C. J. ; Ji W. W. ; Liu Y. ; Chen Y. ; Li Q. ; Li X. ; et al J. Am. Chem. Soc. 2017, 139, 3537. doi: 10.1021/jacs.7b00118
17	Wang H. W. ; Lu Y. ; Zhang B. ; He J. ; Xu H. J. ; Kang Y. S. ; Sun W. Y. ; Yu J. Q. Angew. Chem. Int. Edit. 2017, 56, 7449. doi: 10.1002/anie.201703300
18	Wang C. Q. ; Zhang Y. ; Feng C. Angew. Chem. Int. Edit. 2017, 56, 14918. doi: 10.1002/anie.201708505
19	Wang C. Q. ; Ye L. ; Feng C. ; Loh T. P. J. Am. Chem. Soc. 2017, 139, 1762. doi: 10.1021/jacs.6b12142
20	Tan E. ; Quinonero O. ; Elena de Orbe M. ; Echavarren A. M. ACS Catal. 2018, 8, 2166. doi: 10.1021/acscatal.7b04395
21	Hua Y. ; Asgari P. ; Avullala T. ; Jeon J. J. Am. Chem. Soc. 2016, 138, 7982. doi: 10.1021/jacs.6b04018
22	Wu Y. ; Li W. ; Jiang L. ; Zhang L. ; Lan J. ; You J. Chem. Sci. 2018, 9, 6878. doi: 10.1039/C8SC02529K
23	Lv S. ; Li Y. ; Yao T. ; Yu X. ; Zhang C. ; Hai L. ; Wu Y. Org. Lett. 2018, 20, 4994. doi: 10.1021/acs.orglett.8b01952
24	Zhou X. ; Pan Y. ; Li X. Angew. Chem. Int. Edit. 2017, 56, 8163. doi: 10.1002/anie.201704036
25	Barday M. ; Janot C. ; Halcovitch N. R. ; Muir J. ; Aissa C. Angew. Chem. Int. Edit. 2017, 56, 13117. doi: 10.1002/anie.201706804
26	Wang F. ; Yu X. ; Qi Z. ; Li X. Chem. Eur. J. 2016, 22, 511. doi: 10.1002/chem.201504179
27	Tian M. ; Liu B. ; Sun J. ; Li X. Org. Lett. 2018, 20, 4946. doi: 10.1021/acs.orglett.8b02078
28	Li J. ; Zhang Z. ; Tang M. ; Zhang X. ; Jin J. Org. Lett. 2016, 18, 3898. doi: 10.1021/acs.orglett.6b01916
29	Shen Y. ; Liu G. ; Zhi Z. ; Lu X. Org. Lett. 2013, 15, 3366. doi: 10.1021/ol4014188
30	Xu L. ; Zhu Q. ; Huang G. ; Cheng B. ; Xia Y. J. Org. Chem. 2012, 77, 3017. doi: 10.1021/jo202431q
31	Liu B. ; Fan Y. ; Gao Y. ; Sun C. ; Xu C. ; Zhu J. J. Am. Chem. Soc. 2013, 135, 468. doi: 10.1021/ja3099245
32	Hyster T. K. ; Ruhl K. E. ; Rovis T. J. Am. Chem. Soc. 2013, 135, 5364. doi: 10.1021/ja402274g
33	Duan P. ; Lan X. ; Chen Y. ; Qian S. S. ; Li J. J. ; Lu L. ; Lu Y. ; Chen B. ; Hong M. ; Zhao J. Chem. Commun. 2014, 50, 12135. doi: 10.1039/C4CC05485G
34	Zhang H. ; Wang K. ; Wang B. ; Yi H. ; Hu F. ; Li C. ; Zhang Y. ; Wang J. Angew. Chem. Int. Edit. 2014, 53, 13234. doi: 10.1002/anie.201408555
35	Prakash S. ; Muralirajan K. ; Cheng C. H. Chem. Commun. 2015, 51, 13362. doi: 10.1039/C5CC04211A
36	Hu Z. ; Tong X. ; Liu G. Org. Lett. 2016, 18, 1702. doi: 10.1021/acs.orglett.6b00616
37	García M. P. ; Oro L. A. ; Lahoz F. J. Angew. Chem. Int. Edit. 1988, 27, 1700. doi: 10.1002/anie.198817001
38	Haynes A. ; Mann B. E. ; Morris G. E. ; Maitlis P. M. J. Am. Chem. Soc. 1993, 115, 4093. doi: 10.1021/ja00063a030
39	Lerchen A. ; Knecht T. ; Daniliuc C. G. ; Glorius F. Angew. Chem. Int. Edit. 2016, 55, 15166. doi: 10.1002/anie.201608729
40	Wang X. ; Lerchen A. ; Gensch T. ; Knecht T. ; Daniliuc C. G. ; Glorius F. Angew. Chem. Int. Edit. 2017, 56, 1381. doi: 10.1002/anie.201610117
41	Shin K. ; Kim H. ; Chang S. Acc. Chem. Res. 2015, 48, 1040. doi: 10.1021/acs.accounts.5b00020
42	Yu S. ; Liu S. ; Lan Y. ; Wan B. ; Li X. J. Am. Chem. Soc. 2015, 137, 1623. doi: 10.1021/ja511796h
43	Park Y. ; Heo J. ; Baik M. H. ; Chang S. J. Am. Chem. Soc. 2016, 138, 14020. doi: 10.1021/jacs.6b08211
44	Yang Y. F. ; Houk K. N. ; Wu Y. D. J. Am. Chem. Soc. 2016, 138, 6861. doi: 10.1021/jacs.6b03424
45	Li Y. ; Tang Y. ; He X. ; Shi D. ; Wu J. ; Xu S. Chem. Eur. J. 2017, 23, 7453. doi: 10.1002/chem.201701703
46	Wang Y. ; Chen Y. ; Yang Y. ; Zhou B. Org. Chem. Front. 2018, 5, 1844. doi: 10.1039/C8QO00265G
47	Wang X. ; Lerchen A. ; Daniliuc C. G. ; Glorius F. Angew. Chem. Int. Edit. 2018, 57, 1712. doi: 10.1002/anie.201712019
48	Wang X. ; Li Y. ; Knecht T. ; Daniliuc C. G. ; Houk K. N. ; Glorius F. Angew. Chem. Int. Edit. 2018, 57, 5520. doi: 10.1002/anie.201800803
49	Zhou Z. ; Bian M. ; Zhao L. ; Gao H. ; Huang J. ; Liu X. ; Yu X. ; Li X. ; Yi W. Org. Lett. 2018, 20, 3892. doi: 10.1021/acs.orglett.8b01477
50	Liu G. ; Shen Y. ; Zhou Z. ; Lu X. Angew. Chem. Int. Edit. 2013, 52, 6033. doi: 10.1002/anie.201300881
51	Zhou Z. ; Liu G. ; Shen Y. ; Lu X. Org. Chem. Front. 2014, 1, 1161. doi: 10.1039/C4QO00196F
52	Chen Y. ; Wang D. ; Duan P. ; Ben R. ; Dai L. ; Shao X. ; Hong M. ; Zhao J. ; Huang Y. Nat. Commun. 2014, 5, 4610. doi: 10.1038/ncomms5610
53	Zhou Z. ; Liu G. ; Chen Y. ; Lu X. Org. Lett. 2015, 17, 5874. doi: 10.1021/acs.orglett.5b03060
54	Zhou J. ; Shi J. ; Qi Z. ; Li X. ; Xu H. E. ; Yi W. ACS Catal. 2015, 5, 6999. doi: 10.1021/acscatal.5b01571
55	Xie Y. Chem. Commun. 2016, 52, 12372. doi: 10.1039/c6cc05769a
56	Wang H. ; Wang B. ; Li B. J. Org. Chem. 2017, 82, 9560. doi: 10.1021/acs.joc.7b01566
57	Hu S. ; Lu L. ; Zhu T. ; Wu Q. ; Chen Y. ; Li J. J. ; Zhao J. Org. Biomol. Chem. 2017, 16, 43. doi: 10.1039/C7OB02438J
58	Li Y. ; Shi D. ; Tang Y. ; He X. ; Xu S. J. Org. Chem. 2018, 83, 9464. doi: 10.1021/acs.joc.8b01166
59	Chen W. ; Liu F.-X. ; Gong W. ; Zhou Z. ; Gao H. ; Shi J. ; Wu B. ; Yi W. Adv. Synth. Catal. 2018, 360, 2470. doi: 10.1002/adsc.201800322
60	Zhou W. ; Mei Y. L. ; Li B. ; Guan Z. Y. ; Deng Q. H. Org. Lett. 2018, 20, 5808. doi: 10.1021/acs.orglett.8b02504
61	Yi W. ; Chen W. ; Liu F.-X. ; Zhong Y. ; Wu D. ; Zhou Z. ; Gao H. ACS Catal. 2018, 9508. doi: 10.1021/acscatal.8b02402
62	Pan J. L. ; Xie P. ; Chen C. ; Hao Y. ; Liu C. ; Bai H. Y. ; Ding J. ; Wang L. R. ; Xia Y. ; Zhang S. Y. Org. Lett. 2018, 20, 7131. doi: 10.1021/acs.orglett.8b03082
63	Li M. ; Wang J. H. ; Li W. ; Wen L. R. Org. Lett. 2018, 20, 7694. doi: 10.1021/acs.orglett.8b03427
64	Hu F. ; Xia Y. ; Ye F. ; Liu Z. ; Ma C. ; Zhang Y. ; Wang J. Angew. Chem. Int. Edit. 2014, 53, 1364. doi: 10.1002/anie.201309650
65	Zhou J. ; Shi J. ; Liu X. ; Jia J. ; Song H. ; Xu H. E. ; Yi W. Chem. Commun. 2015, 51, 5868. doi: 10.1039/C5CC00354G
66	Hu Z. ; Liu G. Adv. Synth. Catal. 2017, 359, 1643. doi: 10.1002/adsc.201601296
67	Zhang Y. ; He Y. ; Li L. ; Ji M. ; Li X. Z. ; Zhu G. J. Org. Chem. 2018, 83, 2898. doi: 10.1021/acs.joc.8b00108
68	Wu Y. ; Chen Z. ; Yang Y. ; Zhu W. ; Zhou B. J. Am. Chem. Soc. 2018, 140, 42. doi: 10.1021/jacs.7b10349
69	Duan P. ; Yang Y. ; Ben R. ; Yan Y. ; Dai L. ; Hong M. ; Wu Y.-D. ; Wang D. ; Zhang X. ; Zhao J. Chem. Sci. 2014, 5, 1574. doi: 10.1039/C3SC53228C
70	Li B. ; Lan J. ; Wu D. ; You J. Angew. Chem. Int. Edit. 2015, 54, 1400. doi: 10.1002/anie.201507272
71	Li B. ; Tang G. ; Zhou L. ; Wu D. ; Lan J. ; Zhou L. ; Lu Z. ; You J. Adv. Funct. Mater. 2017, 27, 1605245. doi: 10.1002/adfm.201605245
72	Li B. ; Zhou L. ; Cheng H. ; Huang Q. ; Lan J. ; Zhou L. ; You J. Chem. Sci. 2018, 9, 1213. doi: 10.1039/c7sc04464j
73	Wu Q. ; Chen Y. ; Yan D. ; Zhang M. ; Lu Y. ; Sun W. Y. ; Zhao J. Chem. Sci. 2017, 8, 169. doi: 10.1039/C6SC03169B
74	Xiong F. ; Lu L. ; Sun T. Y. ; Wu Q. ; Yan D. ; Chen Y. ; Zhang X. ; Wei W. ; Lu Y. ; Sun W. Y. ; Li J. J. ; Zhao J. Nat. Commun. 2017, 8, 15912. doi: 10.1038/ncomms15912
75	Wang X. ; Gensch T. ; Lerchen A. ; Daniliuc C. G. ; Glorius F. J. Am. Chem. Soc. 2017, 139, 6506. doi: 10.1021/jacs.7b02725
76	Wu Q. ; Yan D. ; Chen Y. ; Wang T. ; Xiong F. ; Wei W. ; Lu Y. ; Sun W. Y. ; Li J. J. ; Zhao J. Nat. Commun. 2017, 8, 14227. doi: 10.1038/ncomms14227
77	Yan D. ; Wang G. ; Xiong F. ; Sun W. Y. ; Shi Z. ; Lu Y. ; Li S. ; Zhao J. Nat. Commun. 2018, 9, 4293. doi: 10.1038/s41467-018-06763-4

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多功能氧酰胺导向基在碳氢键活化反应中的研究进展

Research Advances in C―H Bond Activation of Multitasking N-Phenoxyamides

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