4 edition of Azosulfones found in the catalog.
January 1, 1982
Written in English
|The Physical Object|
|Number of Pages||49|
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More. Results of the reactions between azosulfones 1 and 3 in DMSO.a Expt Ar Yield of 6 (%)bx I C6H5 (la) 87 2 4-MeC6H4 (l b) 98 3 2-MeC6H4 (lc) 81d 4 4-CIC6H4 (Id) 98 5a NC6H4 (le) 97 5b 11 98d 6 NC6H4 Of) 98 aNu/1 molar ratio = 10, if not otherwise specified.
bYields (vs 1) refer to chromatographically pure products. cTsNH2 always isolated Cited by: 9. provides accurate and independent information on more t prescription drugs, over-the-counter medicines and natural products.
This material is provided for educational purposes only and is not intended for medical Azosulfones book, diagnosis or treatment. Data sources include IBM Watson Micromedex (updated 1 Oct ), Cerner Multum™ (updated 1 Oct ), Wolters Kluwer™.
Book Review: Selected Papers on Molecular Genetics. A Collection of Reprints with Introductory Material. Vol. 1 of the Series “Perspectives in Modern Biology — A Series of Reprint Collections”. By J. Taylor.
Grünewald; Pages: ; First Published: 01 April Journals & Books; Help Such a result appears not to comply with the alleged7 synthetic equivalence between azosulfones and nitrosoarenes and can be reasonably interpreted on the grounds of Scheme 3 (X: COOBut) The formation of the "expected" arylimine 9a by elimination of hydroxide is disfavoured with respect to cyclization onto the.
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Photogeneration of aryl radicals via visible light irradiation of aryl azosulfones; He was also co-author of the book Photochemically-generated intermediates in synthesis (Wiley, ) and coeditor of the book Photoorganocatalysis in Organic Synthesis (World Scientific, ).
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