404597-64-4Relevant academic research and scientific papers
A direct entry to the 1-methoxyindole skeleton and to the corresponding indoles by a novel rearrangement: General syntheses of substituted 1-methoxyindoles
Selvakumar,Reddy, B. Yadi,Azhagan, A. Malar,Khera, Manoj Kumar,Babu, J. Moses,Iqbal, Javed
, p. 7065 - 7069 (2007/10/03)
A short and efficient route to 1-methoxyindoles via a novel rearrangement is disclosed. This route involves only three steps from commercially available nitro compounds. The methodology is also generalized with a variety of examples to afford a series of
Dimethyl malonate as a one-carbon source: A novel method of introducing carbon substituents onto aromatic nitro compounds
Selvakumar,Yadi Reddy,Sunil Kumar,Iqbal, Javed
, p. 8395 - 8398 (2007/10/03)
A number of carbon substituents possessing various functional groups could be introduced onto aromatic nitro compounds using dimethyl malonate as a one-carbon source and linker. Decarboxylation of both the ester groups originating from dimethyl malonate in this methodology is particularly significant.
