(Q60546798)

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A total synthesis of enentiomerically pure vitamin e side chain using a chiral propionate synthon

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A total synthesis of enentiomerically pure vitamin e side chain using a chiral propionate synthon (English)

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Günter Helmchen

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Roland Schmierer

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2

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publication date

January 1983

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published in

Tetrahedron Letters

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volume

24

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issue

12

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page(s)

1235-1238

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cites work

Acyclic stereocontrol through the aldol condensation

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Structure of membrane lipids and physico-biochemical properties of the plasma membrane from Thermoplasma acidophilum, adapted to growth at 37° C

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Enantioselective Generation and Diastereoselective Reactions of Chiral Enolates Derived from ?-Heterosubstituted Carboxylic Acids. Preliminary Communication

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Synthetic studies on (2R,4'R,8'R)-alpha-tocopherol. An approach utilizing side chain synthons of microbiological origin

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7 January 2021

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Syntheses of (2R,4'R,8'R)-alpha-tocopherol and (2R,3'E,7'E)-alpha-tocotrienol

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10.1016/S0040-4039(00)81623-8

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(Q60546798)

A total synthesis of enentiomerically pure vitamin e side chain using a chiral propionate synthon

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