Lewis acid-promoted nitroolefination of enol silyl ethers via an addition elimination process

DOI: 10.1248/cpb.47.394

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 394 - 397 (1999)

Update date:2022-07-29

Topics:

Authors:

Chen, Ji-Jun

Kawabata, Takeo

Ohnishi, Hiroshi

Shang, Muhong

Fuji, Kaoru

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Article abstract of DOI:10.1248/cpb.47.394

Lewis acid-promoted nitroolefination of enol silyl ethers has been developed. Enol ethers 1, 4, 5, and 6 derived from lactones and lactams furnished nitroolefines 2, 7, 8, and 9, respectively in 60 - 99% yields by the treatment with 3 in the presence of L

Full text of DOI:10.1248/cpb.47.394

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