1997
DOI: 10.1016/s0960-894x(97)00314-4
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An efficient synthesis of pyrrolo[2,1-c][1,4]benzodiazepine antibiotics via reductive cyclization

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Cited by 13 publications
(2 citation statements)
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“…To that end we began an investigation in which a series of simple azides were treated with N , N -dimethylhydrazine/ferric chloride. Coincident with the outset of our research, a report by Kamal and co-workers appeared in which a series of azides, when treated with virtually the same reagent/catalyst system, produced the corresponding amines in reasonable yields . While initially disappointed, we soon realized that our initial results were in stark contrast to those of Kamal .…”
Section: Introductionmentioning
confidence: 76%
“…To that end we began an investigation in which a series of simple azides were treated with N , N -dimethylhydrazine/ferric chloride. Coincident with the outset of our research, a report by Kamal and co-workers appeared in which a series of azides, when treated with virtually the same reagent/catalyst system, produced the corresponding amines in reasonable yields . While initially disappointed, we soon realized that our initial results were in stark contrast to those of Kamal .…”
Section: Introductionmentioning
confidence: 76%
“…Since the synthesis of the PBD ring system itself is problematic, due to the labile N10−C11 imine moiety (carbinolamine or methyl ether equivalent), much of the literature to date has focused on the development of new synthetic strategies. , In contrast, very little has been reported about modifications on the PBD ring system or conjugation with carriers . Recently, a C8-linked PBD dimer was prepared 7 which forms a symmetric interstrand cross-link with duplex DNA involving a four-base pair bonding site but spanning six DNA base pairs overall .…”
mentioning
confidence: 99%