Remote C-H Bond Functionalizations. Группа авторовЧитать онлайн книгу.
of meta‐C–H functionalization assisted by directing templates.
Abbreviations
AcacetylAlaL‐alanineArarylBoctert‐butyloxycarbonylBnbenzylBubutylCANceric ammonium nitratecat.catalyticCMDconcerted metalation–deprotonationDCE1,2‐dichloroethaneDGdirecting templateDIH1,3‐diiodo‐5,5‐dimethylhydantoinDMFN,N‐dimethylformamideDMPU1,3‐dimethyl‐3,4,5,6‐tetrahydro‐2(1H)‐pyrimidinoneequivequivalentEDGelectron‐donating templateEWGelectron‐withdrawing templateGlyglycineHFIPhexafluoroisopropanolKIEkinetic isotope effectLligandLDAlithium diisopropylamidemmetaMemethylMPAAmono‐N‐protected amino acidNMPN‐methylpyrrolidinoneoorthopparaPhphenylPheL‐phenylalaninePinpinacolPivpivaloylPrpropylTBAtetrabutylammoniumTFAtrifluoroacetic acidTBAPF6tetrabutylammonium hexafluorophosphateTFEtrifluoroethanolTHFtetrahydrofuranXPhos2,4′,6′‐diisopropyl‐1,1′‐biphenyl‐2‐yldicyclohexylphosphine
References
1 1 Truong, T. and Daugulis, O. (2012). Angew. Chem. Int. Ed. 51: 11677.
2 2 Julia‐Hernandez, F., Simonetti, M., and Larrosa, I. (2013). Angew. Chem. Int. Ed. 52: 11458.
3 3 Ackermann, L. and Li, J. (2015). Nat. Chem. 7: 686.
4 4 Frost, C.G. and Paterson, A.J. (2015). ACS Cent. Sci. 1: 418.
5 5 Li, J., De Sarkar, S., and Ackermann, L. (2016). Top. Organomet. Chem. 55: 217.
6 6 Yang, J. (2015). Org. Biomol. Chem. 13: 1930.
7 7 Chattopadhyay, B. and Bisht, R. (2016). Synlett 27: 2043.
8 8 Dey, A., Agasti, S., and Maiti, D. (2016). Org. Biomol. Chem. 14: 5440.
9 9 Ghosh, M. and De Sarkar, S. (2018). Asian J. Org. Chem. 7: 1236.
10 10 Dey, A., Sinha, S.K., Achar, T.K., and Maiti, D. (2019). Angew. Chem. Int. Ed. 58: 10820.
11 11 Leow, D., Li, G., Mei, T.S., and Yu, J.‐Q. (2012). Nature 486: 518.
12 12 Zhang, Z., Tanaka, K., and Yu, J.‐Q. (2017). Nature 543: 538.
13 13 Achar, T.K., Ramakrishna, K., Pal, T. et al. (2018). Chem. Eur. J. 24: 17906.
14 14 Modak, A., Mondal, A., Watile, R. et al. (2016). Chem. Commun. 52: 13916.
15 15 Li, S., Wang, H., Weng, Y., and Li, G. (2019). Angew. Chem. Int. Ed. https://doi.org/10.1002/anie.201910691.
16 16 Xu, H.‐J., Lu, Y., Farmer, M.E. et al. (2017). J. Am. Chem. Soc. 139: 2200.
17 17 Xu, H.‐J., Kang, Y.‐S., Shi, H. et al. (2019). J. Am. Chem. Soc. 141: 76.
18 18 Wan, L., Dastbaravardeh, N., Li, G., and Yu, J.‐Q. (2013). J. Am. Chem. Soc. 135: 18056.
19 19 Xu, H., Liu, M., Li, L.J. et al. (2019). Org. Lett. 21: 4887.
20 20 Bera, M., Modak, A., Patra, T. et al. (2014). Org. Lett. 16: 5760.
21 21 Deng, Y. and Yu, J.‐Q. (2015). Angew. Chem. Int. Ed. 54: 888.
22 22 Bera, M., Agasti, S., Chowdhury, R. et al. (2017). Angew. Chem. Int. Ed. 56: 5272.
23 23 Jin, Z., Chu, L., Chen, Y.‐Q., and Yu, J.‐Q. (2018). Org. Lett. 20: 425.
24 24 Brochetta, M., Borsari, T., Bag, S. et al. (2019). Chem. Eur. J. 25: 10323.
25 25 Jiao, B., Peng, Z., Dai, Z.‐H. et al. (2019). Eur. J. Org. Chem. 2019: 3195.
26 26 Bag, S., Petzold, M., Sur, A. et al. (2019). Chem. Eur. J. 25: 9433.
27 27 Achar, T.K., Zhang, X., Mondal, R. et al. (2019). Angew. Chem. Int. Ed. 58: 10353.
28 28 Li, S., Cai, L., Ji, H. et al. (2016). Nat. Commun. 7: 10443.
29 29 Fang, L., Saint‐Denis, T.G., Taylor, B.L.H. et al. (2017). J. Am. Chem. Soc. 139: 10702.
30 30 Phipps, R.J. and Gaunt, M.J. (2009). Science 323: 1593.
31 31 Tang, R.‐Y., Li, G., and Yu, J.‐Q. (2014). Nature 507: 215.
32 32 Yang, L., Fu, L., and Li, G. (2017). Adv. Synth. Catal. 359: 2235.
33 33 Wang, B., Zhou, Y., Xu, N. et al. (2019). Org. Lett. 21: 1885.
34 34 Li, S., Ji, H., Cai, L., and Li, G. (2015). Chem. Sci. 6: 5595.
35 35 Yang, G., Lindovska, P., Zhu, D. et al. (2014). J. Am. Chem. Soc. 136: 10807.
36 36 Dutta, U., Modak, A., Bhaskararao, B. et al. (2017). ACS Catal. 7: 3162.
37 37 Yang, G., Zhu, D., Wang, P. et al. (2018). Chem. Eur. J. 24: 3434.
38 38 Bera, M., Maji, A., Sahoo, S.K., and Maiti, D. (2015). Angew. Chem. Int. Ed. 54: 8515.
39 39 Bag, S., Jayarajan, R., Mondal, R., and Maiti, D. (2017). Angew. Chem. Int. Ed. 56: 3182.
40 40 Maji, A., Bhaskararao, B., Singha, S. et al. (2016). Chem. Sci. 7: 3147.
41 41 Bag, S., Jayarajan, R., Dutta, U. et al. (2017). Angew. Chem. Int. Ed. 56: 12538.
42 42 Modak, A., Patra, T., Chowdhury, R. et al. (2017). Organometallics 36: 2418.
43 43 Dai, H.‐X., Li, G., Zhang, X.‐G. et al. (2013). J. Am. Chem. Soc. 135: 7567.
44 44 Mi, R.‐J., Sun, J., Kuhn, F.E. et al. (2017). Chem. Commun. 53: 13209.
45 45 Mi, R.‐J., Sun, Y.‐Z., Wang, J.Y. et al. (2018). Org. Lett. 20: 5126.
46 46 Xu, J., Chen, J., Gao, F. et al. (2019). J. Am. Chem. Soc. 141: 1903.
47 47 Maity, S., Hoque, E., Dhawa, U., and Maiti, D. (2016). Chem. Commun. 52: 14003.
48 48 Lee, S., Lee, H., and Tan, K.L. (2013). J. Am. Chem. Soc. 135: 18778.
49 49 Chu, L., Shang, M., Tanaka, K. et al. (2015). ACS Cent. Sci. 1: 394.
50 50 Zhang, L., Zhao, C., Liu, Y. et al. (2017). Angew. Chem. Int. Ed. 56: 12245.
51 51 Jayarajan, R., Das, J., Bag, S. et al. (2018). Angew. Chem. Int. Ed. 57: 7659.
52 52 Fang, S., Wang, X., Yin, F. et al. (2019). Org. Lett. 21: 1841.
53 53 Patra, T., Watile, R., Agasti, S. et al. (2016). Chem. Commun. 52: 2027.
54 54 Bera, M., Sahoo, S.K., and Maiti, D. (2016). ACS Catal. 6: 3575.
55 55 Yang, Y.‐F., Cheng, G.J., Liu, P. et al. (2014). J. Am. Chem. Soc. 136: 344.
56 56 Cheng, G.‐J., Yang, Y.‐F., Liu, P. et al. (2014). J. Am. Chem. Soc. 136: 894.
Конец ознакомительного фрагмента.
Текст предоставлен ООО «ЛитРес».
Прочитайте эту книгу целиком, купив полную легальную версию на ЛитРес.
Безопасно оплатить книгу можно банковской картой Visa, MasterCard, Maestro, со счета мобильного телефона, с платежного терминала, в салоне МТС или Связной, через PayPal, WebMoney, Яндекс.Деньги, QIWI Кошелек, бонусными картами или другим удобным Вам способом.