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- Visible light photoredox catalysis: regioselective radical addition of aminoalkyl radicals to 2,3-allenoates. Xiaojun Dai, Renjie Mao, Baochuan Guan, Xiaoliang Xu, Xiaonian Li
, RSC Adv.
, 2015
, 5
, 55290
- NHC-catalyzed β-specific addition of N-based nucleophiles to allenoates. Wenchao Wu, Shuangli Xu, Yan Zhang, Xiu Wang, Ruotong Li, Fang Sun, Chenxia Yu, Tuanjie Li, Donghui Wei, Changsheng Yao
, Org. Chem. Front.
, 2020
, 7
, 1593
- Allenes. Part XIX. Synthesis of (±)-hypoglycin A and configuration of the natural isomer. D. K. Black, S. R. Landor
, J. Chem. Soc. C
, 1968
, 288
- Phosphine-catalysed cycloaddition of buta-2,3-dienoates and
but-2-ynoates to [60]fullerene. Bryan F. O’Donovan, Peter B. Hitchcock, Mohamed F. Meidine, Harold W. Kroto, Roger Taylor, David R. M. Walton
, Chem. Commun.
, 1997
, 81
- Highly diastereoselective entry into chiral spirooxindole-based 4-methyleneazetidines via formal [2+2] annulation reaction. G. Rainoldi, M. Faltracco, L. Lo Presti, A. Silvani, G. Lesma
, Chem. Commun.
, 2016
, 52
, 11575
- Convenient synthesis of substituted tetrahydrofuran via Lewis base catalyzed [3 + 2] domino reactions. Yufen Liu, Qi Zhang, Yanlong Du, Aimin Yu, Kui Zhang, Xiangtai Meng
, RSC Adv.
, 2014
, 4
, 52629
- Researches on acetylenic compounds. Part XLV. The alkaline isomerisation of but-3-ynoic acid. G. Eglinton, E. R. H. Jones, G. H. Mansfield, M. C. Whiting
, J. Chem. Soc.
, 1954
, 3197
- Regio- and stereo-selectivity in uncatalysed and catalysed Diels–Alder reactions of allenic esters with furan and 2-methylfuran. M. P. S. Ishar, A. Wali, R. P. Gandhi
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 2185
- DABCO and Bu3P catalyzed [4 + 2] and [3 + 2] cycloadditions of 3-acyl-2H-chromen-ones and ethyl 2,3-butadienoate. Ying Wang, Zhi-Hua Yu, Hu-Fei Zheng, De-Qing Shi
, Org. Biomol. Chem.
, 2012
, 10
, 7739
- 786. Researches on acetylenic compounds. Part LII. The preparation and anomalous absorption spectra of some bicyclo[2 : 2 : 1]-heptane derivatives. E. R. H. Jones, G. H. Mansfield, M. C. Whiting
, J. Chem. Soc.
, 1956
, 4073