Structural elucidation of the cyclic products formed by the reaction of 2,3-O-isopropylidene derivatives of aldehydo-aldose with allylsilanes, vinyl ethers, or vinyl sulfides in the presence of boron trifluoride etherate

DOI: 10.1016/S0040-4039(00)97991-7

Source and publish data:

Tetrahedron Letters p. 5909 - 5912 (1990)

Update date:2022-07-30

Topics:: Authors:

Sugimura

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Article abstract of DOI:10.1016/S0040-4039(00)97991-7

The structural elucidation of the cyclic products derived from 2,3-O-isopropylidene derivatives of aldehydo-aldose and allylsilanes, vinyl ethers, or vinyl sulfides indicated that tetrahydrofuran derivatives were formed by cyclization accompanied with migration of the isopropylidene group.

Full text of DOI:10.1016/S0040-4039(00)97991-7

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Structural elucidation of the cyclic products formed by the reaction of 2,3-O-isopropylidene derivatives of aldehydo-aldose with allylsilanes, vinyl ethers, or vinyl sulfides in the presence of boron trifluoride etherate

DOI: 10.1016/S0040-4039(00)97991-7

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)97991-7

Full text of DOI:10.1016/S0040-4039(00)97991-7

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