Results 1 - 9 of 9

• Jason Siu, Ian R. Baxendale and Steven V. Ley. Microwave assisted Leimgruber–Batcho reaction for the preparation of indoles, azaindoles and pyrroylquinolines, Org. Biomol. Chem., 2004, 2, 160.

  [DOI: 10.1039/b313012f]
  
• [DOI: 10.1021/bi00877a017]
  
• Joule, J. A., Science of Synthesis, (2001) 10, 417.. From 2-(o-Aminoaryl)acetaldehyde Acetals or Hemiacetals, Science of Synthesis
• Takacs, J. M.; Vayalakkada, S., Science of Synthesis, (2001) 1, 359.. Intramolecular Addition of Amine Followed by β-Elimination: In Situ Reduction of Aromatic Nitro Compounds, Science of Synthesis
• Joule, J. A., Science of Synthesis, (2001) 10, 421.. From 2-(o-Nitroaryl)enamines; Leimgruber–Batcho Synthesis, Science of Synthesis
• Joule, J. A., Science of Synthesis, (2001) 10, 517.. Introduction of Aminoalkyl Groups, Science of Synthesis
• Zhang, N.; Dong, D., Science of Synthesis: C-1 Building Blocks in Organic Synthesis, (2013) 2, 336.. Formylation with N-Methylaniline and a Transition-Metal Catalyst, Science of Synthesis
• Joule, J. A., Science of Synthesis Knowledge Updates, (2010) 2, 108.. From 2-(o-Nitroaryl)enamines; Leimgruber–Batcho Synthesis, Science of Synthesis
• Joule, J. A., Science of Synthesis Knowledge Updates, (2010) 2, 258.. Introduction of Aminoalkyl Groups, Science of Synthesis