Zum Mechanismus der nucleophilen Addition an 2,3-Dihydrodipyrrin-1(10H)-one
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
http://link.springer.com/content/pdf/10.1007/BF00809692.pdf
Reference51 articles.
1. Vor der Herausgabe der IUPAC-Empfehlungen zur Nomenklatur von Tetrapyrrolen in: Pure App Chem 59: 779 (1987), wurde diese Substanzklasse als 3,4-Dihydro-5(1H)-pyrromethenone bezeichnet
2. Battersby AR, Fookes CJR, Snow RJ (1984) J Chem Soc Perkin Trans I 1984: 2733
3. Falk H, Grubmayr K, Kapl G, Zrunek U (1982) Monatsh Chem 113: 1329
4. Falk H, Zrunek U (1983) Monatsh Chem 114: 983
5. Grubmayr K (1982) Monatsh Chem 113: 1073
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1. DIPYRRINONES-CONSTITUENTS OF THE PIGMENTS OF LIFE. A REVIEW;Organic Preparations and Procedures International;2006-08
2. The Diels-Alder adduct of phycocyanobilin dimethyl ester and 4-phenyl-1,2,4-triazolin-3,5-dione: A model intermediate for chromatic adaption of biliprotein chromophores?;Tetrahedron Letters;1993-06
3. Syntheses of Bile Pigments. Part 16. Synthesis of a vinyl-substituted 2,3-Dihydrobilinedione: Possible role of this new class of bile pigments in phycobilin biosynthesis;Helvetica Chimica Acta;1989-05-03
4. ChemInform Abstract: Mechanism of the Nucleophilic Addition to 2,3-Dihydrodipyrrin-1(10H)-ones.;ChemInform;1989-02-28
5. Zur intramolekularen nucleophilen Addition von 2,3-Dihydrodipyrrin-1(10H)-onen;Monatshefte f�r Chemie Chemical Monthly;1988
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