Iron (II) triflate as a catalyst for the synthesis of indoles by intramolecular C− H amination
J Bonnamour, C Bolm
Index: Bonnamour, Julien; Bolm, Carsten Organic Letters, 2011 , vol. 13, # 8 p. 2012 - 2014
Full Text: HTML
Citation Number: 70
Abstract
As in other iron catalyses, the solvent played a major role in this reaction. Various solvents were screened, and the results are summarized in Table 1. Reactions performed (with 30 mol % of iron triflate at 80 °C) in DMF, acetonitrile, or protic polar solvents such as water and ethanol gave no product (entries 1−4). In hexane, toluene, and xylene (entries 5−7) as well as other solvents of low polarity, the yields were moderate to good (up to 58% for hexane). Ethers such as ...
Related Articles:
[Huleatt, Paul B.; Lau, Jacelyn; Chua, Sheena; Tan, Yun Lei; Duong, Hung Anh; Chai, Christina L.L. Tetrahedron Letters, 2011 , vol. 52, # 12 p. 1339 - 1342]
[Coowar, Djalil; Bouissac, Julien; Hanbali, Mazen; Paschaki, Marie; Mohier, Eliane; Luu, Bang Journal of Medicinal Chemistry, 2004 , vol. 47, # 25 p. 6270 - 6282]
[Zhu, Zhiqiang; Yuan, Jiangjun; Zhou, Yirong; Qin, Yang; Xu, Jingshi; Peng, Yiyuan European Journal of Organic Chemistry, 2014 , vol. 2014, # 3 p. 511 - 514]
[Gauden; Pezzella; Panzella; Neves-Petersen; Skovsen; Petersen; Mullen; Napolitano; D'Ischia; Sundstroem Journal of the American Chemical Society, 2008 , vol. 130, # 50 p. 17038 - 17043]
[Huleatt, Paul B.; Lau, Jacelyn; Chua, Sheena; Tan, Yun Lei; Duong, Hung Anh; Chai, Christina L.L. Tetrahedron Letters, 2011 , vol. 52, # 12 p. 1339 - 1342]