Two efficient syntheses of (±)-anti-N-benzyl-3-amino-4-hydroxyhexahydroazepine

DOI: 10.1016/0040-4039(95)00623-K

Source and publish data:

Tetrahedron Letters p. 3659 - 3662 (1995)

Update date:2022-07-30

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Authors:

Hu, Hong

Jagdmann Jr., G. Erik

Hughes, Philip F.

Nichols, Jeffrey B.

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Article abstract of DOI:10.1016/0040-4039(95)00623-K

Functionalization of ε-caprolactam or Beckmann rearrangement of the syn-oxime derivative of 3-ethoxy-2-cyclohexen-1-one provided efficient and high-yielding syntheses of (±)-anti-N-benzyl-3-amino-4-hydroxyhexahydroazepine, a key intermediate for the synth

Full text of DOI:10.1016/0040-4039(95)00623-K

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Product name:syn-3-ethoxy-2-cyclohexen-1-one oxime

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