The Carbonylation and Hydroformylation Reactions with Certain Indole Derivatives1
JT Shaw, FT Tyson
Index: Shaw; Tyson Journal of the American Chemical Society, 1956 , vol. 78, p. 2538
Full Text: HTML
Citation Number: 13
Abstract
The reaction of carbon monoxide at elevated pressures and temperatures with the S- potassium salts of various 2-and 3-substituted indole derivatives has been investigated. The results indicate that the indole carbonylation reaction, as it is termed, can be used to prepare 3-indolecarboxaldehydes provided the 2-position is not too hindered sterically or substituted with electron-withdrawing groups. A new compound, N-formylindoline was prepared and ...
Related Articles:
Benzothiazoline: Versatile Hydrogen Donor for Organocatalytic Transfer Hydrogenation
[Saito, Kodai; Shibata, Yukihiro; Yamanaka, Masahiro; Akiyama, Takahiko Journal of the American Chemical Society, 2013 , vol. 135, # 32 p. 11740 - 11743]
Reactivities of nitrenes generated by photolysis of 2-(. omega.-phenylalkyl) phenyl azides
[Murata, Shigeru; Yoshidome, Ryuichi; Satoh, Youji; Kato, Noriyasu; Tomioka, Hideo Journal of Organic Chemistry, 1995 , vol. 60, # 5 p. 1428 - 1434]
The selective hydrogenation of derivatives of pyrrole, indole, carbazole and acridine
[Adkins; Coonradt Journal of the American Chemical Society, 1941 , vol. 63, p. 1563,1568]