DOI: 10.1039/A904333K
(Paper)
Reference Section for: Chem. Commun., 1999, 1589-1590
Unexpected formation of β-lactams and penem isosteres from mesoionics: sequential ring-opening–rearrangement of [3 + 2] cycloadducts
(Note: The full text of this document is currently only available in the PDF Version )
Martín Avalos, Reyes Babiano, Pedro Cintas, José L. Jiménez, Ignacio López, Juan C. Palacios, Michael B. Hursthouse and Mark E. Light
Abstract
A novel and simple method has been developed to obtain penem analogs with biologically interesting functionalities, which combines aromatic aldehydes with thioisomünchnones, a readily available class of mesoionic heterocycles.
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