377-indole ring synthesis

Pyrrole rings frequently serve as precursors to indole rings [37] and PdCl2 induces the oxidative cyclization of pyrrole 37 to a mixture of 38 and 39 [38]. Since the oxidation of tetrahydroindoles to indoles, such as 38 to 39, is usually straightforward, this transformation can be viewed as a novel and efficient indole ring synthesis. 

Hegedus also described an efficient synthesis of 4-bromoindoIe (10) and 4-bromo-l-(4-toluenesulfonyl)indole (11) starting from 2-amino-6-nitrotoluene (9) [20]. The synthesis is lengthy but yields are good, and the method involves the Hegedus indole ring synthesis discussed later in this chapter. 

The incredibly powerful and versatile Heck coupling reaction has found enormous utility in indole ring synthesis and in the elaboration of this important heterocycle. Due to the enormity... 

A different type of indole ring synthesis was accomplished via an intramolecular cyclization of enaminoketones that proceeds through intermediate arylpalladium complexes (90H911). /3-Hydrocarbolines (33) were obtained as the final products. Similar results were obtained in the photo-cyclization of enaminoesters (91TL6129) and enaminolactones (95H1939). Results obtained in the cyclization of A-arylenamines to indoles with... 

Moskalev, N. V. Gribble, G. W. Synthesis and Diels—Alder reactions of the furo[3,4-b]pyrrole ring system. A new indole ring synthesis. Tetrahedron Lett. 2002, 43, 197—201. 

Gribble, G. W. Recent developments in indole ring synthesis-methodology and applications. Perkin 1 2000,1045-1075. 

The incredibly powerful and versatile Heck coupling reaction has found enormous utility in the indole ring synthesis and in the elaboration of this important heterocycle. Due to the enormity of this topic, the section is divided into Heck reactions of indoles, the synthesis of the indole ring as developed by Hegedus, Mori-Ban, and Heck, and the Larock indole ring synthesis. 

Practical methodologies for the synthesis of indoles , Humphrey, G. R. and Kuethe, J. T, Chem. Rev., 2006, 106, 2875 Recent developments in indole ring synthesis-methodology and applications , Gribble, G. W., J. Chem. Soc., Perkin Trans. 1, 2000, 1045. 

Recent developments in indole ring synthesis 00JCS(P1)1045. 

Modification for higher molecular indoles Comparison of steric hindrance on the Fischer indole ring synthesis and the Pfitzinger-Borsche quinoline ring synthesis s. 4, 843... 

For a review of recent methods for indole ring synthesis, see Gribble, G.W. J. Chem. Soc., Perkin Trans. I, 2000, 1045. 

Fukuyama devised a novel tin-mediated indole ring synthesis leading directly to 2-stannylindoles that can capture aryl and alkyl halides in a Pd-catalyzed crosscoupling termination reaction [110-112]. The presumed pathway is illustrated and involves initial tributylstannyl radical addition to the isonitrile 65, cyclization, and final formation of stannylindole 66. 

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