[1]
Chen, Y.; Gao, L.; Feng, M.; Gu, L.; He, N.; Wang, J.; Araki, Y.; Blau, W.; Ito, O. Photophysical and optical limiting properties of axially modified phthalocyanines. Mini Rev. Org. Chem., 2009, 6(1), 55-65.
[http://dx.doi.org/10.2174/157019309787316166]
[http://dx.doi.org/10.2174/157019309787316166]
[2]
Feng, X. Electronic characters and synthesis method of novel conjugated system based on benzodithiophene groups. Mini Rev. Org. Chem., 2019, 16(3), 216-227.
[http://dx.doi.org/10.2174/1570193X15666180412152056]
[http://dx.doi.org/10.2174/1570193X15666180412152056]
[3]
Agrawal, N.; Arora, B. Self-Healing polymers and composites: Extrinsic routes. Mini Rev. Org. Chem., 2022, 19(4), 496-512.
[http://dx.doi.org/10.2174/1570193X18666210802110810]
[http://dx.doi.org/10.2174/1570193X18666210802110810]
[4]
Deng, G.; Wang, Q.; Yang, M.; Li, B.; Han, T.; Chang, B.; Li, X.; Zhang, X.; Li, Z. Synthesis and modifications of electron-withdrawing groups based on multi-cyano heterocyclics. Mini Rev. Org. Chem., 2019, 16(3), 208-215.
[http://dx.doi.org/10.2174/1570193X15666180412151523]
[http://dx.doi.org/10.2174/1570193X15666180412151523]
[5]
Zhang, R.; Jin, X.; Wen, X.; Chen, Q. Recent advance in 1-D organic semiconductors for waveguide applications. Mini Rev. Org. Chem., 2019, 16(3), 244-252.
[http://dx.doi.org/10.2174/1570193X15666180406143727]
[http://dx.doi.org/10.2174/1570193X15666180406143727]
[6]
Gao, W.; Liu, J.; Kityk, I. The progress in the field auxiliary donors and their application in novel organic second-order nonlinear optical chromophores. Mini Rev. Org. Chem., 2019, 16(3), 228-235.
[http://dx.doi.org/10.2174/1570193X15666180627150155]
[http://dx.doi.org/10.2174/1570193X15666180627150155]
[7]
Raut, J.; Sahoo, P. Detection of biothiols using some novel chemosensors: An overview. Mini Rev. Org. Chem., 2021, 18(7), 867-884.
[http://dx.doi.org/10.2174/1570193X17999201109212903]
[http://dx.doi.org/10.2174/1570193X17999201109212903]
[8]
Panja, S.; Ghosh, K. Progress in benzimidazole/benzimidazolium-derived supramolecular gelators in ion recognition. Mini Rev. Org. Chem., 2020, 17(8), 1042-1055.
[http://dx.doi.org/10.2174/1570193X17999200430090415]
[http://dx.doi.org/10.2174/1570193X17999200430090415]
[9]
Gouda, M.; Abu-Hashem, A.; Abdelgawad, A. Thieno[3,2-c] quinoline heterocyclic synthesis and reactivity part (VI). Mini Rev. Org. Chem., 2022, 19(5), 629-653.
[http://dx.doi.org/10.2174/1570193X18666211004102537]
[http://dx.doi.org/10.2174/1570193X18666211004102537]
[10]
Walunj, Y.; Mhaske, P.; Kulkarni, P. Application, reactivity and synthesis of isoxazole derivatives. Mini Rev. Org. Chem., 2021, 18(1), 55-77.
[http://dx.doi.org/10.2174/1570193X17999200511131621]
[http://dx.doi.org/10.2174/1570193X17999200511131621]
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