| Literature DB >> 29711794 |
Christopher Cox1, Harald Wack1, Thomas Lectka1.
Abstract
N-Protonated amides have been proposed as intermediates in several biologically important reactions, but they have yet to be identified spectroscopically. The first step toward this goal is now reported in the form of spectroscopic and crystallographic proof of a strong intramolecular hydrogen bond between a charged proton donor and an amide nitrogen atom in the "proton sponge" derivative 1; novel reactivity results from this interaction. TfO-= trifluoromethanesulfonate. © 1999 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.Entities:
Keywords: Amides; Hydrogen bonding; Naphthalenes; Proton sponges
Year: 1999 PMID: 29711794 DOI: 10.1002/(SICI)1521-3773(19990315)38:6<798::AID-ANIE798>3.0.CO;2-W
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336