An efficient and diastereoselective [2+2] cycloaddition: Convenient and enantioselective route to trans-2',3'-dihydroxymethylcyclobutane nucleoside analogs

DOI: 10.1016/0040-4039(91)85023-X

Source and publish data:

Tetrahedron Letters p. 6997 - 7000 (1991)

Update date:2022-07-30

Topics:: Authors:

Ahmad

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Article abstract of DOI:10.1016/0040-4039(91)85023-X

An efficient route to (2S-trans)-2,3-bis[(benzoyloxy)methyl]cyclobutanone (3a), a key intermediate in the synthesis of cyclobutane nucleoside analogs, via a novel asymmetric [2+2] cycloaddition, is described.

Full text of DOI:10.1016/0040-4039(91)85023-X

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Article Doi

An efficient and diastereoselective [2+2] cycloaddition: Convenient and enantioselective route to trans-2',3'-dihydroxymethylcyclobutane nucleoside analogs

DOI: 10.1016/0040-4039(91)85023-X

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0040-4039(91)85023-X

Full text of DOI:10.1016/0040-4039(91)85023-X

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