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Publikováno v:
Organic Process Research & Development. 9:792-799
Prodrugs derived from the β-lactamase inhibitor 6-β-hydroxymethylsulbactam can be synthesized efficiently in a three-step process by making use of the highly stereoselective radical debromination utilizing tri-n-butylgermanium hydride. This reagent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df16dc73ecd755f647b398bc12d7d270
https://doi.org/10.1021/op050151s
https://doi.org/10.1021/op050151s
