13C Nuclear Magnetic Resonance Studies. 47. 13C Spectra of some exo-Methylenecycloalkanes and -norbornanes

1975 ◽  
Vol 53 (4) ◽  
pp. 589-595 ◽  
Author(s):  
S. H. Grover ◽  
J. B. Stothers

The shielding effects of the exo-methylene group on neighboring carbons in several cycloalkanes, methylcyclohexanes, and in the norbornane ring system have been characterized by 13C n. m. r. examination of 28 compounds. The results are compared with those for the carbonyl group and the utility of these data for structural elucidations is discussed. The more distinctive trends exhibited by the methyl carbons in these systems are compared with those for cyclohexanes, cyclohexanones, norbornanes, and norcamphors.


1977 ◽  
Vol 55 (5) ◽  
pp. 841-848 ◽  
Author(s):  
J. B. Stothers ◽  
C. T. Tan

The 13C nmr spectra of a series of 20 bicyclo[3.2.1]octanols and -octenols have been determined to examine the shielding effects of the hydroxyl group on the skeletal carbons in this ring system. For comparison, the previously unreported data for a few closely related alcohols in the [2.1.1], [2.2.1], and [3.2.2] systems were also collected. The utility of these substituent effects for configuraional and conformational assignments is discussed.



Tetrahedron ◽  
2001 ◽  
Vol 57 (49) ◽  
pp. 9789-9798 ◽  
Author(s):  
Shawn R Hitchcock ◽  
George P Nora ◽  
David M Casper ◽  
Michael D Squire ◽  
Christopher D Maroules ◽  
...  


1974 ◽  
Vol 52 (10) ◽  
pp. 1973-1982 ◽  
Author(s):  
Howard Charles Clark ◽  
Leo Ernest Manzer ◽  
John Edward Henry Ward

The 13C n.m.r. parameters for thirteen di- and trimethylplatinum(IV) derivatives have been obtained. It is shown that the 13C shieldings and 1JPtC and 2JPtCH values of methyl groups both cis and trans to varied ligands consistently follow trends similar to those found for related methylplatinum(II) derivatives.



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