Synthesis
Efficient Preparation of Polyfunctional Indoles via a Zinc Organometallic Variation of the Fischer Indole Synthesis
ZG Zhang, BA Haag, JS Li, P Knochel
Index: Synthesis, , # 1 p. 23 - 29
Full Text: HTML
Citation Number: 6
Abstract
... Subsequent N-alkylation of the intermediate 1p [t-BuOK (1.2 equiv), 0 ˚C, 20 min; then Cl(CH 2 ) 3 ... During the new indole synthesis, a range of sensitive functional groups such as nitro, ester, cyano, and keto groups ... s, 1 H), 7.77 (d, J = 8.4 Hz, 1 H), 7.24 (d, J = 8.4 Hz, 1 H), 2.67 (s ...
Related Articles:
A microwave-assisted, propylphosphonic anhydride (T3P®) mediated one-pot Fischer indole synthesis
[Tetrahedron Letters, , vol. 52, # 34 p. 4417 - 4420]