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- The mechanism and impact of mono/bis(iodoimidazolium) halogen bond donor catalysts on Michael addition of indole with trans-crotonophenone: DFT calculations. Yuanyuan Sun, Ying Li, Xiaoyan Li, Yanli Zeng
, Phys. Chem. Chem. Phys.
, 2022
, 24
, 6690
- Tandem additions of 3,4-dihydroisoquinolines to γ-hydroxy-α,β-unsaturated ketones: a green and new access to oxazolo[2,3-a]tetrahydroisoquinolines. Sheng-Han Huang, Yu-Wei Shih, Wen-Tse Huang, Deng-Hong Li, Te-Fang Yang
, RSC Adv.
, 2016
, 6
, 91870
- Acidic-functionalized ionic liquid as an efficient, green and reusable catalyst for hetero-Michael addition of nitrogen, sulfur and oxygen nucleophiles to α,β-unsaturated ketones. Feng Han, Lei Yang, Zhen Li, Chungu Xia
, Org. Biomol. Chem.
, 2012
, 10
, 346
- Synthesis of an enol-ether of a cyclopropanone from a diazoalkenylether: a novel class of compound. David P. G. Hamon, Kevin M. Pullen
, J. Chem. Soc., Chem. Commun.
, 1975
, 459a
- Bromonium salts: diaryl-λ3-bromanes as halogen-bonding organocatalysts. Yasushi Yoshida, Seitaro Ishikawa, Takashi Mino, Masami Sakamoto
, Chem. Commun.
, 2021
, 57
, 2519
- Copper(i)-catalyzed asymmetric [3 + 2] cycloaddition of N-ester acylhydrazones and β-trifluoromethyl-α,β-unsaturated ketones. Bo Zhu, Huihui Fan, Yanan Ding, Yubing Zhai, Le Wang, Mengqi Wang, Gongming Zhu, Junbiao Chang
, Org. Chem. Front.
, 2022
, 9
, 5544
- Asymmetric tandem Michael addition–ylide olefination reaction for the synthesis of optically active cyclohexa-1,3-diene derivatives. Long-Wu Ye, Shou-Bing Wang, Qing-Gang Wang, Xiu-Li Sun, Yong Tang, Yong-Gui Zhou
, Chem. Commun.
, 2009
, 3092
- The potential of pnicogen bonding for catalysis – a computational study. J. Schmauck, M. Breugst
, Org. Biomol. Chem.
, 2017
, 15
, 8037
- A halogen-bonding-catalyzed Michael addition reaction. Jan-Philipp Gliese, Stefan H. Jungbauer, Stefan M. Huber
, Chem. Commun.
, 2017
, 53
, 12052
- A computational study on the stereoselective organocatalytic epoxidation of α,β-unsaturated aldehydes with hydrogen peroxide. Filipe J. S. Duarte, A. Gil Santos
, Org. Biomol. Chem.
, 2013
, 11
, 7179