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Synthesis of 6-epi-trehazolin from D-ribonolactone: Evidence for the non-existence of a 5,6-ringfused structural isomer of 6-epi-trehazolin

DOI: 10.1016/S0040-4039(00)75990-9

Source and publish data:

Tetrahedron Letters p. 887 - 890 (1994)

Update date:2022-09-26

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Authors:

Shiozaki, MasaoShiozaki, Masao

Kobayashi, YoshiyukiKobayashi, Yoshiyuki

Arai, MasamiArai, Masami

Haruyama, HideyukiHaruyama, Hideyuki

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Article abstract of DOI:10.1016/S0040-4039(00)75990-9

6-Epi-trehazolin was synthesized in a stereocontrolled manner, and this synthesis provided proof for the non-existence of oxazine structural isomer of 6-epi-trehazolin.

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Full text of DOI:10.1016/S0040-4039(00)75990-9

Products guided by the article

Product name:<1S-(1α,4α,5α)>-3-<<(tert-Butyldimethylsilyl)oxy>methyl>-4,5-(isopropylidenedioxy)-1-<(4-methoxybenzyl)oxy>-2-cyclopentene

Cas No:160343-87-3

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