Bldg 201-BS-07, Proton and carbon-I 3 assignments based on long-range coupling to the methyl protons are reported for the three isomeric N-methyldiazabenzene salts. All resolved "J,, coupling constants are reported.
Determination of the sign of long-range 1H–13C scalar coupling constants to non-protonated carbons: application to assignment
✍ Scribed by Yasuhiro Kumaki; Kunio Hikichi
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 84 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The sign of the scalar coupling between a carbonyl carbon and ˛-proton J(C 0 ,H ˛), for the cyclic dipeptide cyclo(Leu-Gly) was determined relative to that between an amide proton and ˛-proton 3 J(H N ,H ˛) by an E.COSYtype HSQC experiment. The pulse sequence used in this experiment gives a cross peak between the amide proton and carbonyl carbon which shows an E.COSY-type tilt caused by the ˛-proton. The sign information on J(C 0 ,H ˛) was used to distinguish between two-bond (intra-residue) and three-bond (inter-residue) J(C 0 ,H ˛)s, leading to the assignment of the carbonyl carbons of the cyclic dipeptide cyclo(Leu-Gly).
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