A New Access to Isoindolo[2,1-b][2,4]benzodiazepines through an N -Acyliminium Ion - Amide Cyclization
Identifieur interne : 001275 ( France/Analysis ); précédent : 001274; suivant : 001276A New Access to Isoindolo[2,1-b][2,4]benzodiazepines through an N -Acyliminium Ion - Amide Cyclization
Auteurs : Pascal Pigeon [France] ; Bernard Decroix [France]Source :
- Tetrahedron Letters [ 0040-4039 ] ; 1997.
Abstract
Isoindolo[2,10b][2,4]benzodiazepines 11a–c were synthesized from hydroxylactam-acid 5 when it was treated successively with thionyl chloride, ammonia (or an alkylamine) and p-toluenesulfonic acid. © 1997 Elsevier Science Ltd.
Url:
DOI: 10.1016/S0040-4039(97)00539-X
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 000290
- to stream Istex, to step Curation: 000290
- to stream Istex, to step Checkpoint: 000C83
- to stream Main, to step Merge: 001D92
- to stream Main, to step Curation: 001D40
- to stream Main, to step Exploration: 001D40
- to stream France, to step Extraction: 001275
Links to Exploration step
ISTEX:78BE9B553187E66FFA409F0310452817B823A7F5Le document en format XML
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<front><div type="abstract" xml:lang="en">Isoindolo[2,10b][2,4]benzodiazepines 11a–c were synthesized from hydroxylactam-acid 5 when it was treated successively with thionyl chloride, ammonia (or an alkylamine) and p-toluenesulfonic acid. © 1997 Elsevier Science Ltd.</div>
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