๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

3JSnCCH(o) and 13C NMR of some new neutral and anionic complexes of Ph3SnNCO

โœ Scribed by P.C. Srivastava; A. Trivedi


Book ID
103907767
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
269 KB
Volume
48
Category
Article
ISSN
1386-1425

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


1H- and 13C-NMR. Studies of some metal c
โœ Paul S. Pregosin; Eginhard Steiner ๐Ÿ“‚ Article ๐Ÿ“… 1979 ๐Ÿ› John Wiley and Sons ๐ŸŒ German โš– 215 KB ๐Ÿ‘ 1 views

## Abstract The aromatic ^1^Hโ€ and ^13^Cโ€NMR. spectra of some metal complexes of o, oโ€ฒโ€dihydroxyazobenzenes are shown to be useful in distinguishing the two possible isomers (acolar and discolar) stemming from the non equivalence of the two ligating azo nitrogen atoms. The ortho aromatic carbon ato

77Se and 13C NMR spectroscopy of some 1,
โœ Helmut Duddeck; Torsten Hotopp ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 264 KB

## Abstract ^77^Se and ^13^C chemical shift of 19 1,2,3โ€selenadiazoles are discussed in terms of substituent effects and conformaโ€tional behaviour of the molecules. It is shown that the ^77^Se chemical shifts of such compounds are suitable tools for chiral discrimination in diastereomeric compounds

13C NMR spectra of some 1-, 3- and 4-mon
โœ A. van Veldhuizen; M. van Dijk; Georgine M. Sanders ๐Ÿ“‚ Article ๐Ÿ“… 1980 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 419 KB

## Abstract Chemical shifts and substituent chemical shift (SCS) effects are reported for 21 monosubstituted isoโ€quinolines, carrying a halogeno, amino, piperidino or ethoxy group in position 1, 3 or 4. In some cases, assignments of ^13^C resonances were based on the spectra of the corresponding 5โ€

Studies in the synthesis of C-ring bridg
โœ Victoria F. Roche; Donald L. Nagel; Edward B. Roche ๐Ÿ“‚ Article ๐Ÿ“… 1985 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 507 KB

The "C NMR spectra of eight novel derivatives of bicydo[2.2.2]-and -[3.2.l]octane have been recorded and analysed. Tbese compounds were isolated and characterized as intermediates in the synthesb of a unique derivative of 1,2,3,3a,llb,llc-hexahydroahydroaporphine. Carbon chemical shift assignments o