Relevant bibliographies by topics / Mevinic acids synthesis][Compactin

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Mevinic acids synthesis][Compactin'

Author: Grafiati
Published: 4 June 2021
Last updated: 16 February 2022

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Journal articles on the topic "Mevinic acids synthesis][Compactin"

1

Rosen, Terry, and Clayton H. Heathcock. "The synthesis of mevinic acids." Tetrahedron 42, no. 18 (1986): 4909–51. http://dx.doi.org/10.1016/s0040-4020(01)88045-5.

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2

Bennett, Frank, Garry Fenton, and David W. Knight. "Synthesis of conformationally restricted relatives of the mevinic acids." Tetrahedron 50, no. 17 (1994): 5147–58. http://dx.doi.org/10.1016/s0040-4020(01)90425-9.

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3

Narasaka, Koichi, Masatoshi Saitou, and Nobuharu Iwasawa. "Asymmetric synthesis of the hydronaphthalene moieties of mevinic acids." Tetrahedron: Asymmetry 2, no. 12 (1991): 1305–18. http://dx.doi.org/10.1016/s0957-4166(00)80028-2.

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4

McCague, Ray, Horacio F. Olivo, and Stanley M. Roberts. "Enantioselective synthesis of the hydroxy-lactone moiety of mevinic acids." Tetrahedron Letters 34, no. 23 (1993): 3785–86. http://dx.doi.org/10.1016/s0040-4039(00)79228-8.

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5

France, Christopher J., Ian M. McFarlane, Christopher G. Newton, Philippe Pitchen, and Michael Webster. "Straightforward homochiral synthesis of the lactone moiety of mevinic acids." Tetrahedron Letters 34, no. 10 (1993): 1635–38. http://dx.doi.org/10.1016/0040-4039(93)85028-u.

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6

BENNETT, F., G. FENTON, and D. W. KNIGHT. "ChemInform Abstract: Synthesis of Conformationally Restricted Relatives of the Mevinic Acids." ChemInform 25, no. 39 (2010): no. http://dx.doi.org/10.1002/chin.199439264.

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7

NARASAKA, K., M. SAITOU, and N. IWASAWA. "ChemInform Abstract: Asymmetric Synthesis of the Hydronaphthalene Moieties of Mevinic Acids." ChemInform 23, no. 15 (2010): no. http://dx.doi.org/10.1002/chin.199215305.

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8

MCCAGUE, R., H. F. OLIVO, and S. M. ROBERTS. "ChemInform Abstract: Enantioselective Synthesis of the Hydroxy-Lactone Moiety of Mevinic Acids." ChemInform 24, no. 43 (2010): no. http://dx.doi.org/10.1002/chin.199343136.

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9

Enders, Dieter, та Frank Burkamp. "α-Heterosubstituted Aldehydes in Organic Synthesis. Enantioselective Approaches to New Analogues of Mevinic Acids". Collection of Czechoslovak Chemical Communications 68, № 5 (2003): 975–1006. http://dx.doi.org/10.1135/cccc20030975.

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Abstract:
Various aldol approaches towards the asymmetric synthesis of the lactone moiety of HMG-CoA-reductase inhibitors are described. Auxiliary controlled as well as catalytic aldol reactions resulted only in modest to low selectivities, whereas 1,2-additions to readily available highly enantiomerically enriched α-heterosubstituted aldehydes yielded δ-hydroxy-β-ketoesters with a high degree of diastereocontrol and in good chemical yields. The novel mevinic acid analogues could then be obtained bysyn-reduction of the addition products.
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10

Kumar, Archana, and Donald C. Dittmer. "Synthesis of Intermediates for the Lactone Moiety of Mevinic Acids via Tellurium Chemistry." Journal of Organic Chemistry 59, no. 17 (1994): 4760–64. http://dx.doi.org/10.1021/jo00096a017.

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Dissertations / Theses on the topic "Mevinic acids synthesis][Compactin"

1

Khodabocus, A. "Synthetic approach to the AB rings of forskolin." Thesis, University of Manchester, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234201.

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