RING EXPANSION REACTIONS IN THE FORMATION OF MACROCYCLIC LACTAMS. A SYNTHESIS OF DESOXO-INANDENINE

DOI: 10.1016/S0040-4039(01)80211-2

Source and publish data:

Tetrahedron Letters p. 2205 - 2208 (1984)

Update date:2022-09-26

Topics:

Authors:

Waelchli, Rudolf

Guggisberg, Armin

Hesse, Manfred

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Article abstract of DOI:10.1016/S0040-4039(01)80211-2

Desoxo-inandenine, a reduction product of the macrocyclic spermidine alkaloids inandenin-12-one and -13-one has been synthesized from 2-nitro-cyclotridecanone by ring expansion reactions including a Zip reaction step.

Full text of DOI:10.1016/S0040-4039(01)80211-2

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