## Abstract The dipeptide alanylproline has been prepared with the proline residue both ^13^C (15%) and ^15^N (95%) enriched. ^15^N NMR spectra of alanylproline reveal signals for both possible conformations—__cis__ and __trans__—of the dipeptide backbone in solution. Different p__K__ values for bo
Carbon-13 chemical shifts and 13C15N coupling constants of 3,4-dihydroisoquinoline-15N, its 15N-oxide and their conjugate acids
✍ Scribed by Manfred Christl
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 189 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
On protonation of 3,4‐dihydroisoquinoline‐^15^N ^1^J(^13^C—1, ^15^N) is increased by a factor of five and ^1^J(^13^C—3, ^15^N) changes its sign, while on protonation of 3,4‐dihydroisoquinoline‐^15^N‐oxide the coupling constants, including the relatively large ^1^J(^13^C—1, ^15^N), remain practically constant, although significant alterations of the ^13^C chemical shifts take place.
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