The SELective INverse detection of carbon-proton CORrelation pulse sequence that yields a 1D spectrum of a proton directly bonded to a selected carbon resonance has been converted into a proton and carbon double-selective variant that provides a (1)H spectrum of a selected proton that is long-range coupled to a specific carbon resonance. The resulting 1D proton multiplet exhibits a pure absorptive in-phase lineshape for precise measurement of specific long-range proton-carbon coupling constants in small organic molecules at natural abundance.
Keywords: 13C; 1H; HSQMBC; NMR; SELINCOR; in-phase multiplets; long-range proton-carbon coupling constants.
Copyright © 2011 John Wiley & Sons, Ltd.