Chapter 5.2: Five-Membered Ring Systems: Pyrroles and Benzo Analogs

作者: Erin T. Pelkey , Jonathon S. Russel

DOI: 10.1016/S0959-6380(08)80008-6

关键词:

摘要: Publisher Summary This chapter discusses pyrroles and benzo analogs. Pyrroles indoles are amongst the most studied heterocyclic ring systems because of their diverse biological activity materials science applications. Pyrrole rings important structural subunits recognition elements found in a number bioactive materials, including small molecule natural products tetrapyrroles (i.e., porphyrins) related macrocycles. The also recent implementation traditional methods development novel strategies for synthesis indole alkaloids. isolation characterization new alkaloids remains fruitful avenue discovery agents with potential biomedical application. Oxindoles spirocyclic variants represent general class that have received considerable attention as synthetic targets, well key intermediates product synthesis. Strategies core structures several been reported. In developing biomimetic approach toward haplophytine, Corey co-workers investigated direct coupling two partners form an aspidophytine mimic tetracyclic canthiphytine analog.

参考文章(1,037)
Florea Dumitraşcu, Dan George Dumitrescu, Pyrrolo[1,2-b]pyridazines. A revisit Arkivoc. ,vol. 2008, ,(2008) , 10.3998/ARK.5550190.0009.109
Michael C. Hewitt, Liming Shao, Synthesis of 2-phenyl indoxyls Arkivoc. ,vol. 2006, ,(2006) , 10.3998/ARK.5550190.0007.B03
J. A. Ellman, The Direct Approach Science. ,vol. 316, pp. 1131- 1132 ,(2007) , 10.1126/SCIENCE.1143373
Yuan-Qing Fang, Robert Karisch, Mark Lautens, Efficient syntheses of KDR kinase inhibitors using a Pd-catalyzed tandem C-N/Suzuki coupling as the key step. Journal of Organic Chemistry. ,vol. 72, pp. 1341- 1346 ,(2007) , 10.1021/JO062228W
Michael T. Huggins, Patrick S. Barber, David Florian, William Howton, Short, Efficient Syntheses of Pyrrole α-Amides Synthetic Communications. ,vol. 38, pp. 4226- 4239 ,(2008) , 10.1080/00397910802323130
Rubén Martín, Catharine H. Larsen, Ana Cuenca, Stephen L. Buchwald, Cu-catalyzed tandem C-N bond formation for the synthesis of pyrroles and heteroarylpyrroles. Organic Letters. ,vol. 9, pp. 3379- 3382 ,(2007) , 10.1021/OL7014225
Elizabeth R. Blair, Hillary E. Hoffman, Anthony C. Bishop, Engineering non-natural inhibitor sensitivity in protein tyrosine phosphatase H1 Bioorganic & Medicinal Chemistry. ,vol. 14, pp. 464- 471 ,(2006) , 10.1016/J.BMC.2005.08.025
Yoshiaki Nakao, Shiro Ebata, Akira Yada, Tamejiro Hiyama, Masashi Ikawa, Sensuke Ogoshi, Intramolecular arylcyanation of alkenes catalyzed by nickel/AlMe2Cl. Journal of the American Chemical Society. ,vol. 130, pp. 12874- 12875 ,(2008) , 10.1021/JA805088R
Xuemei Zhang, Irene Lee, Xiang Zhou, Anthony J. Berdis, Hydrophobicity, Shape, and π-Electron Contributions During Translesion DNA Synthesis Journal of the American Chemical Society. ,vol. 128, pp. 143- 149 ,(2006) , 10.1021/JA0546830