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Sundberg

Heller E J, Sundberg R L and Tanner D J 1982 Simple aspects of Raman scattering J. Rhys. Chem. 86 1822-33... [Pg.279]

Carey Sundberg Chapter 13.1 problems 1 2 3a, b, c Smith Chapter 7... [Pg.57]

Aromatic Substitution (Carey Sundberg, Chapter 11) Intramolecular Wittig Reaction Sigmatropic Rearrangements... [Pg.167]

Sundberg, R. J. 1970, 77ie Chemistry of Indoles, Academic Press New York London Svoboda, M. Zavada, J. Sicher, J. 1965, Coll. Czech. Chem. Commun. 30, 413 Swem, D. 1953, Org. Reaa. (N. Y.) 7, 378... [Pg.380]

A -(2 2-Diethoxyethyl)anilines are potential precursors of 2,3-unsubstituted indoles. A fair yield of 1-methylindole was obtained by cyclization of N-inethyl-M-(2,2-diethoxyethyl)aniline with BFj, but the procedure failed for indole itself[2], Nordlander and co-workers alkylated anilines with bromo-acetaldehyde diethyl acetal and then converted the products to N-trifliioro-acetyl derivatives[3]. These could be cyclized to l-(trifluoroacetyl)indoles in a mixture of trifluoroacetic acid and trifluoroacetic anhydride. Sundberg and... [Pg.41]

Best Synthetic Methods is now 10 years old, is a family of 16 volumes and has been well received by the majority of chemists as a valuable aid in their synthetic endeavours, be they academic or commercial. The focus of the series so far has been on special methods, reagents or techniques. This volume is the first of a new sub-series with a focus on heterocycles and their synthesis. It is amazing the extent to which each heterocyclic type has its own specialized synthetic methodology. Whether the chemist is endeavouring to make a heterocycle by ring synthesis or wishes to introduce specific substituents, it is the intention that this new development will serve their needs in a practical, authoritative, fully illustrative and compact manner. Richard Sundberg is an authority on indole chemistry and it is a pleasure to have such a noted heterocyclist to initiate this venture. [Pg.181]

R] Sundberg, R. J. The Chemistry of Indoles, Acaxlemic Press New York London, 1970. [Pg.109]

Sundberg and Bloom reported that methyl or ethyl 2-(l-benzenesulfonylindol-2-yl)acrylate (17) on heating with both l-methoxycarbonyl-l,2-dihydropyridine... [Pg.273]

The previously unknown 2-nitroindoles have been conveniently prepared from o-nitroben-zaldehyde via the Sundberg indole synthesis fEq 10 61 ... [Pg.343]


See other pages where Sundberg is mentioned: [Pg.5]    [Pg.30]    [Pg.151]    [Pg.26]    [Pg.26]    [Pg.44]    [Pg.60]    [Pg.98]    [Pg.98]    [Pg.102]    [Pg.141]    [Pg.164]    [Pg.164]    [Pg.182]    [Pg.89]    [Pg.90]    [Pg.365]    [Pg.443]    [Pg.443]    [Pg.396]    [Pg.730]    [Pg.831]    [Pg.630]    [Pg.87]    [Pg.310]    [Pg.311]    [Pg.311]    [Pg.170]    [Pg.170]    [Pg.180]    [Pg.116]    [Pg.361]   
See also in sourсe #XX -- [ Pg.43 , Pg.269 , Pg.615 , Pg.956 ]

See also in sourсe #XX -- [ Pg.33 , Pg.221 , Pg.626 ]

See also in sourсe #XX -- [ Pg.33 , Pg.221 , Pg.626 ]




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Cadogan-Sundberg indole synthesis

Cadogan-Sundberg indole synthesis applications

Cadogan-Sundberg indole synthesis carbazoles

Carbazoles Sundberg indole synthesis

Cyclization Cadogan-Sundberg indole synthesis

Indoles Cadogan-Sundberg synthesis

Sundberg indole preparation

Sundberg indole synthesis

Sundberg indole synthesis applications

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