1,4-Remote stereocontrol via asymmetric [2,3]-Wittig rearrangements

DOI: 10.1016/0040-4039(95)00397-U

Source and publish data:

Tetrahedron Letters p. 2789 - 2792 (1995)

Update date:2022-07-30

Topics:: Authors:

Tomooka, Katsuhiko

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Article abstract of DOI:10.1016/0040-4039(95)00397-U

The carbanion rearrangement of the propargylic ether of the β-(1-alkoxyethyl) allyl alcohol was found to proceed with a high degree of either 1,4-syn or 1,4-anti selection by virtue of the proper choice of the combination of the alkoxy group with the solv

Full text of DOI:10.1016/0040-4039(95)00397-U

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Article Doi

1,4-Remote stereocontrol via asymmetric [2,3]-Wittig rearrangements

DOI: 10.1016/0040-4039(95)00397-U

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0040-4039(95)00397-U

Full text of DOI:10.1016/0040-4039(95)00397-U

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