+++RCS_(New J. Chem; Org. Chem. Front; Org. Biomol. Chem.)_5_статей

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Добрый день!

Пожалуйста, помогите скачать следующие статьи:

1. Visible-light-induced tandem difluoroalkylated spirocyclization of N-arylpropiolamides: access to C3-difluoroacetylated spiro[4,5]trienones
J.-W. Yuan, L. Shen, M.-Y. Ma, S. Feng, W.Yang, L.-R. Yang, Y.-M. Xiao, S.-R. Zhang, L.-B. Qu
New J. Chem., 2022,46, 4470-4482

Код: Выделить всё

https://doi.org/10.1039/D2NJ00131D

2. Trifluoromethylthiolative spirocyclization of biaryl ynones without leaving groups on the para-position of dearomatized aryl rings
Y. Liang, S. Wang, H. Jia, B. Chen, F. Zhuc, Z. Huo
New J. Chem., 2022,46, 12077-12081

Код: Выделить всё

https://doi.org/10.1039/D2NJ01056A

3. Metal-free dearomatization reactions of naphthol-ynamides for the divergent and enantioselective synthesis of azaspirocycles
H.-H. Li, Y.-P. Zhang, T.-Y. Zhai, B.-Y. Liu, C.-Y. Shi, J.-M. Zhoua, L.-W. Ye
Org. Chem. Front., 2022,9, 3709-3717

Код: Выделить всё

https://doi.org/10.1039/D2QO00685E

4. Rapid synthesis of spirodienones via electrochemical dearomative spirocyclization in flow
N. Li, Z. Shi, Y. Yuan, Z. Li, K.-Y. Ye
Org. Chem. Front., 2022,9, 6586-6591

Код: Выделить всё

https://doi.org/10.1039/D2QO01392D

5. Synthesis of polychloromethylated and halogenated spiro[5,5]trienones via dearomative spirocyclization of biaryl ynones
J.-N. Li, Z.-J. Li, L.-Y. Shen, P. Li, Y. Zhangc, W.-C. Yang
Org. Biomol. Chem., 2022,20, 6659-6666

Код: Выделить всё

https://doi.org/10.1039/D2OB01053D

Спасибо!

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