(Q56036203)

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New syntheses of optically active vitamin E side chain by chemicoenzymatic approach

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New syntheses of optically active vitamin E side chain by chemicoenzymatic approach (English)

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G. Speranza

4

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Paola Gramatica

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P. Gramatica

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1

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P. Manitto

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2

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D. Monti

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3

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publication date

January 1986

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published in

Tetrahedron

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volume

42

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issue

24

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page(s)

6687-6692

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cites work

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

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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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https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2982109-8

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7 January 2021

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Synthetic studies on (2R,4'R,8'R)-alpha-tocopherol. Facile syntheses of optically active, saturated, acyclic isoprenoids via stereospecific [3,3]sigmatropic rearrangements

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Synthetic studies on (2R,4'R,8'R)-alpha-tocopherol. An alternative synthesis of (2R,6R)-(+)-2,6,10-trimethylundecan-1-ol, a key side chain synthon

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

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7 January 2021

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Stereospecific reduction of geraniol to (R)-(+)-citronellol bySaccharomyces cerevisiae

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10.1016/S0040-4020(01)82109-8

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(Q56036203)

New syntheses of optically active vitamin E side chain by chemicoenzymatic approach

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