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- Usual and unusual reactions of cyclohexane-1,2-dione with aryl azides and amines: a structural corrigendum. Neeraj Singh, Klaus Banert
, New J. Chem.
, 2017
, 41
, 1897
- Regioselective or enantiogenic electrochemical and microbial reductions of 1,2-diketones. Patrick Boutoute, Guy Mousset, Henri Veschambre
, New J. Chem.
, 1998
, 22
, 247
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Direct preparation of diacetals from 1,2-diketones and their use as
1,2-diol protecting groups
. Achim Hense, Steven V. Ley, Helen M. I. Osborn, Dafydd R. Owen, Jean-François Poisson, Stuart L. Warriner, Kieron E. Wesson
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 2023
- Chiral indane skeleton based thiourea catalyzed highly stereoselective cascade Michael–enolation–cyclization reaction. Qiao Ren, Yaojun Gao, Jian Wang
, Org. Biomol. Chem.
, 2011
, 9
, 5297
- Functional diversity of organic molecule enzyme cofactors. Michael Richter
, Nat. Prod. Rep.
, 2013
, 30
, 1324
- Syntheses using monoketals of cyclohexane-1: 2-dione. Part I. 2-Oxocyclohexane-1-spiro-2′-1′: 3′-dioxolan and the corresponding oxathiolan and dithiolan. R. H. Jaeger, Herchel Smith
, J. Chem. Soc.
, 1955
, 160
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Preparation, structure, derivatisation and NMR data of
cyclohexane-1,2-diacetal protected carbohydrates
. Peter Grice, Steven V. Ley, Jörg Pietruszka, Henning W. M. Priepke, Stuart L. Warriner
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 351
- Expeditious assembly of fused dihydropyranones via N-heterocyclic carbene-catalyzed tandem Michael addition/lactonization. Qiao Ren, Muyao Li, Lujiang Yuan
, Org. Biomol. Chem.
, 2017
, 15
, 1329
- Stabilization of singlet ethoxycarbonylnitrene by 1,4-dioxan. Part 4. Yield of nitrene products in 1,4-dioxan–cyclohexane and effect of cyclohexane-1,2-dione on C–H insertion. Hiroshi Takeuchi, Toshikazu Nishiyama, Michiharu Mitani, Teruko Tsuchida, Kikuhiko Koyama
, J. Chem. Soc., Perkin Trans. 2
, 1979
, 839
- 368. Physical properties and chemical constitution. Part XL. The electrical dipole moments of some cyclic diketones. C. W. N. Cumper, G. B. Leton, A. I. Vogel
, J. Chem. Soc.
, 1965
, 2067