CYCLOADDITIONS IN SYNTHESES.PART 41. CHIRAL SPIROCYCLIC 5-ARYL-METHYLENE-1,3-DIOXANE-4,6-DIONES AS NOVEL SYNTHONS FOR ENANTIOMERICALLY PURE 2-ARYLCYCLOPROPANE-1,1-DICARBOXYLATES

DOI: 10.1016/S0040-4039(01)93764-5

Source and publish data:

Tetrahedron Letters p. 5281 - 5284 (1989)

Update date:2022-07-31

Topics:

Authors:

Sato, Masayuki

Hisamichi, Hiroyuki

Kaneko, Chikara

Suzaki, Naoko

Furuya, Toshio

Inukai, Noriyoshi

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Article abstract of DOI:10.1016/S0040-4039(01)93764-5

E- and Z- isomers of spirocyclic 5-arylmethylene-1,3-dioxane-4,6-dione, useful synthons for enantiomerically pure cyclopropane-1,1-dicarboxylates, have been synthesized from 1-menthone.Their diastereofacial selectivity is explained by a boat conformation in their dioxanedione ring.

Full text of DOI:10.1016/S0040-4039(01)93764-5

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Product name:1,5-Dioxaspiro[5.5]undecane-2,4-dione, 10-methyl-7-(1-methylethyl)-3-[(4-nitrophenyl)methylene]-, (6S,7S,10R)-

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