One-pot synthesis of tetrahydro-pyrrolobenzodiazepines and tetrahydro-pyrrolobenzodiazepinones through sequential 1,3-dipolar cycloaddition/ N -alkylation ( N -acylation)/Staudinger/aza-Wittig reactions
A new synthetic method for diastereoselective synthesis of tetrahydro-pyrrolo[1,2- d ][1,4]benzodiazepines and tetrahydro-pyrrolo[1,2- d ][1,4]diazepinones is developed which involves 1,3-dipolar cycloaddition, N -alkylation or N -acylation and Staudinger/aza-Wittig reactions. This one-pot and three...
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Veröffentlicht in: | Green chemistry : an international journal and green chemistry resource : GC 2019, Vol.21 (16), p.4489-4494 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | A new synthetic method for diastereoselective synthesis of tetrahydro-pyrrolo[1,2-
d
][1,4]benzodiazepines and tetrahydro-pyrrolo[1,2-
d
][1,4]diazepinones is developed which involves 1,3-dipolar cycloaddition,
N
-alkylation or
N
-acylation and Staudinger/aza-Wittig reactions. This one-pot and three-step synthesis of four components gave two different heterocyclic scaffolds. Green chemistry metrics analysis of the reaction process provided favorable results. |
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ISSN: | 1463-9262 1463-9270 |
DOI: | 10.1039/C9GC01642B |