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- CCXVI.—Studies in the n-butyl series. Part I. Aryl n-propyl ketones. Gilbert T. Morgan, Wilfred John Hickinbottom
, J. Chem. Soc., Trans.
, 1921
, 119
, 1879
- CXLIII.—ortho- and meta-Derivatives of simple alkyl phenyl ketones. Leslie Alderman Elson, Charles Stanley Gibson, John Dobney Andrew Johnson
, J. Chem. Soc.
, 1930
, 1128
- Different hybridized oxygen atoms controlled chemoselective formation of oxocarbenium ions: synthesis of chiral heterocyclic compounds. Xiao-Na Wu, Zhi-Hao You, Yan-Kai Liu
, Org. Biomol. Chem.
, 2018
, 16
, 6507
- Enantioselective conjugate hydrosilylation of α,β-unsaturated ketones. Huan Yang, Guanglin Weng, Dongmei Fang, Changjiang Peng, Yuanyuan Zhang, Xiaomei Zhang, Zhouyu Wang
, RSC Adv.
, 2019
, 9
, 11627
- Organocatalyzed highly stereoselective Michael addition of ketones to alkylidene malonates and nitroolefins using chiral primary-secondary diamine
catalysts based on bispidine. Jie Liu, Zhigang Yang, Xiaohua Liu, Zhen Wang, Yanling Liu, Sha Bai, Lili Lin, Xiaoming Feng
, Org. Biomol. Chem.
, 2009
, 7
, 4120
- Microwave-enhanced radical reactions at ambient temperature Part 3: Highly selective radical synthesis of 3-cyclohexyl-1-phenyl-1-butanone in a microwave double cylindrical cooled reactor. Satoshi Horikoshi, Junichi Tsuzuki, Masatsugu Kajitani, Masahiko Abe, Nick Serpone
, New J. Chem.
, 2008
, 32
, 2257
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N-Heterocyclic carbene-catalyzed aza-Michael addition. Qiang Kang, Yugen Zhang
, Org. Biomol. Chem.
, 2011
, 9
, 6715
- Index of subjects
, J. Chem. Soc., Abstr.
, 1921
, 120
, ii841
- Rhodium(i)-catalyzed 1,4-conjugate arylation toward β-fluoroalkylated electron-deficient alkenes: a new entry to a construction of a tertiary carbon center possessing a fluoroalkyl group. Atsunori Morigaki, Tomoo Tanaka, Tomotsugu Miyabe, Takashi Ishihara, Tsutomu Konno
, Org. Biomol. Chem.
, 2013
, 11
, 586
- Simple iodoalkyne-based organocatalysts for the activation of carbonyl compounds. Juan V. Alegre-Requena, Alberto Valero-Tena, Isaac G. Sonsona, Santiago Uriel, Raquel P. Herrera
, Org. Biomol. Chem.
, 2020
, 18
, 1594