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- Vilsmeier–Haack reagent mediated synthetic transformations with an immobilized iridium complex photoredox catalyst. Peng Zhi, Zi-Wei Xi, Dan-Yan Wang, Wei Wang, Xue-Zheng Liang, Fei-Fei Tao, Run-Pu Shen, Yong-Miao Shen
, New J. Chem.
, 2019
, 43
, 709
- Synthesis and characterization of semiaromatic polyamides with dicyclohexane units. Guang-ming Yan, Gang Zhang, Hao-hao Ren, Yan Li, Jie Yang
, RSC Adv.
, 2016
, 6
, 76490
- Semi-aromatic polyamides containing methylene and thioether units: synthesis and membrane properties. Gang Zhang, Su-Jiao Cao, Hao-Hao Ren, Xiao-Jun Wang, Sheng-Ru Long, Jie Yang
, RSC Adv.
, 2016
, 6
, 99184
- Reactivity of (poly)fluorobenzamides in palladium-catalysed direct arylations. Nouria Laidaoui, Mian He, Douniazad El Abed, Jean-François Soulé, Henri Doucet
, RSC Adv.
, 2016
, 6
, 62866
- Semiaromatic polyamides containing ether and different numbers of methylene (2–10) units: synthesis and properties. Gang Zhang, Yu-xuan Zhou, Yu Kong, Zhi-min Li, Sheng-Ru Long, Jie Yang
, RSC Adv.
, 2014
, 4
, 63006
- Iodoferrocene as a partner in N-arylation of amides. Lingaswamy Kadari, William Erb, Thierry Roisnel, Palakodety Radha Krishna, Florence Mongin
, New J. Chem.
, 2020
, 44
, 15928
- Palladium-catalyzed regio- and chemoselective ortho-benzylation of C–H bond using a functionalizable primary amide directing group: a concise synthesis of dibenzo[b,e]azepin-6-ones. Joydev K. Laha, Pooja U. Shah, Krupal P. Jethava
, Chem. Commun.
, 2013
, 49
, 7623
- Efficient synthesis of N-(buta-2,3-dienyl) amides from terminal N-propargyl amides and their synthetic potential towards oxazoline derivatives. Bo Chen, Nan Wang, Wu Fan, Shengming Ma
, Org. Biomol. Chem.
, 2012
, 10
, 8465
- ortho-Amide-directed 2,4-dibromohydration of conjugated enynes. Yu-Chao Wang, Rui-Xiang Wang, Guanyinsheng Qiu, Hongwei Zhou, Wenlin Xie, Jin-Biao Liu
, Org. Chem. Front.
, 2019
, 6
, 2471
- Application of W-band 19F electron nuclear double resonance (ENDOR) spectroscopy to distance measurement using a trityl spin probe and a fluorine label. N. B. Asanbaeva, A. A. Sukhanov, A. A. Diveikina, O. Y. Rogozhnikova, D. V. Trukhin, V. M. Tormyshev, A. S. Chubarov, A. G. Maryasov, A. M. Genaev, A. V. Shernyukov, G. E. Salnikov, A. A. Lomzov, D. V. Pyshnyi, E. G. Bagryanskaya
, Phys. Chem. Chem. Phys.
, 2022
, 24
, 5982