The substituent effect on stereoselective reductive lithiation of 4,5-disubstituted 2-phenylthiooxolane

DOI: 10.1246/cl.1998.409

Source and publish data:

Chemistry Letters p. 409 - 410 (1998)

Update date:2022-08-03

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Authors:

Amano, Seiji

Fujiwara, Kenshu

Murai, Akio

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Article abstract of DOI:10.1246/cl.1998.409

In the reductive lithiation of 2-phenylthiooxolane system, the coexistence of the substituents at C2 and C3 with cis-configuration was found to increase the ratio of 2,5-trans-2-lithiooxolane to 2,5-cis derivative.

Full text of DOI:10.1246/cl.1998.409

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