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- Ruthenium-catalyzed direct C3 alkylation of indoles with α,β-unsaturated ketones. Shuai-Shuai Li, Hui Lin, Xiao-Mei Zhang, Lin Dong
, Org. Biomol. Chem.
, 2015
, 13
, 1254
- Synthesis of α-hydroxy ketones and vicinal (R,R)-diols by Bacillus clausii DSM 8716T butanediol dehydrogenase. Lukas Muschallik, Denise Molinnus, Melanie Jablonski, Carina Ronja Kipp, Johannes Bongaerts, Martina Pohl, Torsten Wagner, Michael J. Schöning, Thorsten Selmer, Petra Siegert
, RSC Adv.
, 2020
, 10
, 12206
- A chemoselective α-aminoxylation of aryl ketones: a cross dehydrogenative coupling reaction catalysed by Bu4NI. Yogesh Siddaraju, Kandikere Ramaiah Prabhu
, Org. Biomol. Chem.
, 2015
, 13
, 11651
- Palladium-catalyzed enolate arylation as a key C–C bond-forming reaction for the synthesis of isoquinolines. Ben S. Pilgrim, Alice E. Gatland, Carlos H. A. Esteves, Charlie T. McTernan, Geraint R. Jones, Matthew R. Tatton, Panayiotis A. Procopiou, Timothy J. Donohoe
, Org. Biomol. Chem.
, 2016
, 14
, 1065
- Nickel catalyzed α-arylation of ketones with aryltrimethylammonium triflates. Jing Li, Zhong-Xia Wang
, Org. Biomol. Chem.
, 2016
, 14
, 7579
- Regio- and enantio-selective oxidation of diols by Candida parapsilosis ATCC 7330. Thakkellapati Sivakumari, Anju Chadha
, RSC Adv.
, 2014
, 4
, 60526
- Iodine promoted α-hydroxylation of ketones. Yogesh Siddaraju, Kandikere Ramaiah Prabhu
, Org. Biomol. Chem.
, 2015
, 13
, 6749
- A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones. Victor-Emmanuel H. Kassin, Romain Morodo, Thomas Toupy, Isaline Jacquemin, Kristof Van Hecke, Raphaël Robiette, Jean-Christophe M. Monbaliu
, Green Chem.
, 2021
, 23
, 2336
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α-Arylation of ketones by aryllead triacetates. Effect of methyl
and phenyl substitution at the α position
. Jacqueline Morgan, John T. Pinhey, Bruce A. Rowe
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 1005
- One-pot synthesis of acyloxy carbonyl compounds from ketones using a Pybox–copper(ii) catalyst. Wei-Guo Jia, Hui Zhang, Dan-Dan Li, Li-Qin Yan
, RSC Adv.
, 2016
, 6
, 27590