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Banwell

Banwell C N and Primas H 1963 On the analysis of high-resolution nuclear magnetic resonance spectra. I. Methods of calculating NMR spectra Mol. Phys. 6 225-56... [Pg.2112]

C N Banwell, Fundamentals of Molecular Spectroscopy, 3rd edn, McGraw-Hill, London, 1983... [Pg.814]

The only physical property which has been studied for substituted vinylidene sets is the nmr chemical shift of the vinylidene proton in substituted ethylenes and in tra s-l,2-disubstituted ethylenes. The first attempt at correlating chemical shift data for substituted ethylenes with the Hammett equation appears to be the work of Banwell and Sheppard (53), who reported a correlation of A2 values with the or constants, the A2 values being defined by the equation... [Pg.93]

Banwell EF, Abelardo ES, Adams DJ et al (2009) Rational design and application of responsive alpha-helical peptide hydrogels. Nat Mater 8 596-600... [Pg.163]

Banwell, C.N. and McCash E.M., Molekiilspektroskopie, R. Oldenbourg Verlag, Munchen, 1999, 417 (translated from Fundamentals of Molecular Spectroscopy, 4th ed., McGraw-Hill International, U.K., 1994). [Pg.20]

Banwell, M.G. (1996) Cyclopropyl Compounds as Chemical Building Blocks Total Syntheses of the Alkaloids (—)-Colchicine, Imerubrine and Grandirubrine. Pure and Applied Chemistry, 68,... [Pg.191]

Banwell JG, Kistel LA, Giannella RA, Weber FL, Lieber A, Powell DE Small intestine bacterial overgrowth syndrome. Gastroenterology 1981 80 834-845. [Pg.108]

M. Banwell, A. Edwards, J. Smith, E. Hamel, P. Verdier-Pinard, J. Chem. Soc, Perkin Trans. [Pg.128]

Scheme 9 First Banwell Group Synthesis of Lamellarin Natural Products... Scheme 9 First Banwell Group Synthesis of Lamellarin Natural Products...
Banwell s group has provided an alternative strategy [32] for obtaining the lamellarin framework and it is presented in Scheme 10. The methodology involves the formation of a 2,4-disubstituted pyrrole (53) containing an acid... [Pg.80]

Banwell, Steglich and Kashman [62,63] have combined their expertise to complete a total synthesis of halitulin and this is described in Scheme 29. [Pg.101]

Scheme 29 Banwell, Steglich and Kashman Synthesis of Halitulin Natural Products... Scheme 29 Banwell, Steglich and Kashman Synthesis of Halitulin Natural Products...
Banwell M, Flynn B, Hamel E, Hockless D (1997) Chem Commun 2 207... [Pg.104]

Banwell M, Bray A, Edwards A, Wong D (2002) J Chem Soc Perkin Trans 1 11 1340... [Pg.105]

See other pages where Banwell is mentioned: [Pg.385]    [Pg.385]    [Pg.30]    [Pg.361]    [Pg.362]    [Pg.92]    [Pg.274]    [Pg.274]    [Pg.214]    [Pg.739]    [Pg.1165]    [Pg.1704]    [Pg.1704]    [Pg.183]    [Pg.483]    [Pg.246]    [Pg.313]    [Pg.197]    [Pg.393]    [Pg.140]    [Pg.434]    [Pg.65]    [Pg.156]    [Pg.165]    [Pg.166]    [Pg.172]    [Pg.69]    [Pg.71]    [Pg.75]    [Pg.79]    [Pg.81]    [Pg.105]    [Pg.105]    [Pg.105]    [Pg.480]   
See also in sourсe #XX -- [ Pg.29 , Pg.377 , Pg.378 ]



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Intramolecular Diels-Alder Reactions Platencin (Banwell), Platensimycin (Matsuo), (-)-Halenaquinone (Trauner), ()-Cassaine (Deslongchamps)

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