scholarly journals Sphingolipid bases. A revisitation of the O-methyl derivatives of sphingosine. Isolation and characterization of diacetate derivatives, with revised 13C nuclear magnetic resonance assignments for D-erythro-sphingosine.

1995 ◽  
Vol 36 (4) ◽  
pp. 787-803
Author(s):  
A Kisic ◽  
M Tsuda ◽  
R J Kulmacz ◽  
W K Wilson ◽  
G J Schroepfer
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Resonance Assignments ◽  
Isolation And Characterization ◽  
13C Nuclear Magnetic Resonance ◽  
Methyl Derivatives ◽  
Derivatives Of ◽  
Nuclear Magnetic

13C Nuclear Magnetic Resonance Studies. Part 48. 13C Spectra of a Variety of Bicyclic Ketones

1975 ◽  
Vol 53 (9) ◽  
pp. 1351-1361 ◽  
Author(s):  
S. H. Grover ◽  
D. H. Marr ◽  
J. B. Stothers ◽  
C. T. Tan
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Important Influence ◽  
Magnetic Resonance Studies ◽  
Methyl Substitution ◽  
13C Nuclear Magnetic Resonance ◽  
Bicyclic Ketones ◽  
Methyl Derivatives ◽  
Derivatives Of ◽  
Nuclear Magnetic

The 13C n.m.r. spectra of a series of 37 bicyclic ketones have been recorded to examine the variations in 13C shieldings with structure and with methyl substitution. Several examples of six skeletal types were included: bicyclo[4.4.0]decanones, bicyclo[4.1.0]heptanones, bicyclo-[3.1.0]hexanones, bicyclo[3.2.2]nonanones, bicyclo[3.2.1]- and -[3.3.0]octanones as well as bicyclo[2.1.1]hexan-2-one, nopinone (6,6-dimethylbicyclo[3.1.1]heptan-2-one), and two methyl derivatives of the latter. The observed trends associated with methyl substitution follow well-defined patterns and offer further support for the application of 13C shieldings as aids for stereochemical assignments especially through the well known γ effects. The variation in the shieldings of the carbonyl carbons in these systems suggested that bond eclipsing interactions have an important influence on this parameter. With this notion, the heretofore puzzling variations observed for the cycloalkanones are readily interprétable in terms of their favored conformations.

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