Academic literature on the topic 'Darzens condensation'

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Journal articles on the topic "Darzens condensation"

1

Tanaka, Koichi, and Ryusuke Shiraishi. "Darzens condensation reaction in water." Green Chemistry 3, no. 3 (2001): 135–36. http://dx.doi.org/10.1039/b102412b.

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2

BANSAL, R. K., and V. K. SHARMA. "ChemInform Abstract: Steric Effects in the Darzens Condensation." ChemInform 23, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.199244173.

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3

Roy, Joyeeta, Tanushree Mal, Supriti Jana, and Dipakranjan Mal. "Regiodefined synthesis of brominated hydroxyanthraquinones related to proisocrinins." Beilstein Journal of Organic Chemistry 12 (March 16, 2016): 531–36. http://dx.doi.org/10.3762/bjoc.12.52.

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Dibromobenzoisofuranone 12, synthesized in six steps, was regiospecifically annulated with 5-substituted cyclohexenones 13/36 in the presence of LiOt-Bu to give brominated anthraquinones 14/38 in good yields. Darzens condensation of 30 was shown to give chain-elongated anthraquinone 32. Alkaline hydrolysis of 38 furnished 39 representing desulfoproisocrinin F.
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4

Arai, Shigeru, and Takayuki Shioiri. "Catalytic asymmetric Darzens condensation under phase-transfer-catalyzed conditions." Tetrahedron Letters 39, no. 15 (1998): 2145–48. http://dx.doi.org/10.1016/s0040-4039(98)00081-1.

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5

Sulmon, Paul, Norbert De Kimpe, Niceas Schamp, Jean Paul Declercq, and Bernard Tinant. "A novel Darzens-type condensation using .alpha.-chloro ketimines." Journal of Organic Chemistry 53, no. 19 (1988): 4457–62. http://dx.doi.org/10.1021/jo00254a007.

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6

Mamedov, V. A., E. A. Berdnikov, S. Tsuboi, et al. "Substituted benzaldehydes in the darzens condensation with alkyl dihaloacetates." Russian Chemical Bulletin 55, no. 8 (2006): 1455–63. http://dx.doi.org/10.1007/s11172-006-0440-7.

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7

Svoboda, Jiří, Miloslav Nič, and Jaroslav Paleček. "An Anomalous Course of the Darzens Reaction Catalyzed with Magnesium Methoxide." Collection of Czechoslovak Chemical Communications 57, no. 1 (1992): 119–22. http://dx.doi.org/10.1135/cccc19920119.

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The reaction of benzaldehyde with methyl chloroacetate catalyzed with magnesium methoxide gave beside the expected methyl 2,3-epoxy-3-phenylpropanoate (I) also comparable amounts of methyl 2-hydroxy-3-methoxy-3-phenylpropanoate (II). The condensation was accompanied by a competing disproportionation of benzaldehyde giving methyl benzoate and benzyl alcohol. The course of the condensation reaction is discussed.
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8

Baldoli, Clara, Paola Del Buttero та Stefano Maiorana. "Asymmetric Darzens condensation on chiral η6Cr(CO)3 complexed benzaldehydes". Tetrahedron 46, № 23 (1990): 7823–30. http://dx.doi.org/10.1016/s0040-4020(01)90079-1.

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9

Krafft, Marie E., Steven J. R. Twiddle та John W. Cran. "The Darzens condensation of α,β-unsaturated aldehydes and ketones". Tetrahedron Letters 52, № 12 (2011): 1277–80. http://dx.doi.org/10.1016/j.tetlet.2011.01.046.

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10

Rekhter, M. A. "ChemInform Abstract: Synthesis of 2-Acylindoles by the Darzens Condensation." ChemInform 33, no. 30 (2010): no. http://dx.doi.org/10.1002/chin.200230141.

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