Rearrangement of spiro [2H-1-benzopyran-2,2 '-[2H] indoles] to pyrrolo[1,2-a]indole derivatives
Författare
Summary, in English
Heating of 1'-(N-substituted carbamoyl)methylspiro[2H-1-benzopyran-2,2'-[2H]indoles] with potassium hydroxide in ethanol yields diastereomeric 5a,13-methano-6H-1,3-benzoxazepino[3,2-a]indole-12-carboxamides. Reduction of the latter with sodium borohydride affords 1,2,3,9a-tetrahydro-2-hydroxyaryl-9H-pyrrolo[1,2-a]indole-3-carboxamides .
Avdelning/ar
Publiceringsår
2002
Språk
Engelska
Sidor
1123-1128
Publikation/Tidskrift/Serie
Journal of Heterocyclic Chemistry
Volym
39
Issue
6
Dokumenttyp
Artikel i tidskrift
Förlag
Journal of Heterocyclic Chemistry
Ämne
- Organic Chemistry
Status
Published
ISBN/ISSN/Övrigt
- ISSN: 0022-152X