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Palladium-catalyzed chemoselective synthesis of indane-1,3-dione derivatives via tert -butyl isocyanide insertion . Huaqing Duan, Zhong Chen, Li Han, Yulin Feng, Yongming Zhu, Shilin Yang
, Org. Biomol. Chem.
, 2015
, 13
, 6782
Mechanochemically assisted morphing of shape shifting polymers . Rui Tang, Wenli Gao, Yulin Jia, Kai Wang, Barun Kumar Datta, Wei Zheng, Huan Zhang, Yuanze Xu, Yangju Lin, Wengui Weng
, Chem. Sci.
, 2023
, 14
, 9207
Hydrazinolysis of 2-phenyl-2-(phthalimidoalkyl)indan-1,3-diones . Trevor A. Crabb, Ansuya Patel, Roger F. Newton, Trevor J. Cholerton
, J. Chem. Soc., Perkin Trans. 1
, 1985
, 191
CuBr-mediated synthesis of 1,4-naphthoquinones via ring expansion of 2-aryl-1,3-indandiones . Xu Zhang, Di Wang, Mengfan Chang, Wanya Wang, Zhi Shen, Xuefeng Xu
, Chem. Commun.
, 2023
, 59
, 12326
Reactions of lndane-1,3-diones with 1,4-naphthoquinones . Katherine Buggle, John A. Donnelly, Lorcan J. Maher
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 1006
Syntheses and transformations of α-azido
ketones and related derivatives . Tamás Patonay, Krisztina Kónya, Éva Juhász-Tóth
, Chem. Soc. Rev.
, 2011
, 40
, 2797
Synthesis of 1,2,3,9b-tetrahydro-9b-hydroxy-1-phenylpyrrolo[2,1-a ]isoindol-5-one via the hydrazinolysis of 2-phenyl-2(2-phthalimidoethyl)indan-1,3-dione . Trevor A. Crabb, Ansuya Patel, Roger F. Newton, Barry J. Price, Michael J. Tucker
, J. Chem. Soc., Perkin Trans. 1
, 1982
, 2783
A facile copper(i )-catalyzed homo-coupling of indanone derivatives using diaziridinone under mild conditions . Wenyong Han, Yihui Yang, Yingguang Zhu, Yian Shi
, Org. Biomol. Chem.
, 2019
, 17
, 6998
Original papers on pharmaceutical analysis . I. W. Macleod, R. A. Wiggins, P. A. Haywood, G. Munro, S. M. Vaughan, J. Harfield, J. C. Deavin, J. Terry, I. M. Beaumont, A. C. Mehta, W. S. Brickell, R. D. Gifford, P. B. Baker, R. Fowler
, Proc. Anal. Div. Chem. Soc.
, 1978
, 15
, 329
Recent advances in transition-metal-catalyzed carbene insertion to C–H bonds . Yuan He, Zilong Huang, Kaikai Wu, Juan Ma, Yong-Gui Zhou, Zhengkun Yu
, Chem. Soc. Rev.
, 2022
, 51
, 2759