Fused lactones as a route to functionalized 1-substituted indoles

DOI: 10.1002/jhet.5570310614

Source and publish data:

Journal of Heterocyclic Chemistry p. 1381 - 1384 (1994)

Update date:2022-07-29

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Authors:

Schuster

Coppola Coppola

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Article abstract of DOI:10.1002/jhet.5570310614

Indole lactones 8 and 14 were synthesized as a means of functionalizing the 1-isopropyl substituent of the indole nucleus. Lactone 8, upon reduction with diisobutylaluminum hydride, produces lactol 9 which behaves like a masked hydroxy aldehyde and underg

Full text of DOI:10.1002/jhet.5570310614

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