The reduction of organic nitro compounds by carbon monoxide as an effective strategy for the synthesis of N-heterocyclic compounds: a personal account-Reference-Cited by-同舟云学术

The reduction of organic nitro compounds by carbon monoxide as an effective strategy for the synthesis of N-heterocyclic compounds: a personal account

Published:2017-01-30 Issue:S1 Volume:28 Page:97-115
ISSN:2037-4631
Container-title:Rendiconti Lincei
language:en
Short-container-title:Rend. Fis. Acc. Lincei

Author:

Ferretti Francesco,Formenti Dario,Ragaini Fabio^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Earth and Planetary Sciences,General Agricultural and Biological Sciences,General Environmental Science

Link

http://link.springer.com/article/10.1007/s12210-017-0601-7/fulltext.html

Reference104 articles.

1. Adam W, Krebs O (2003) The nitroso ene reaction: a regioselective and stereoselective allylic nitrogen functionalization of mechanistic delight and synthetic potential. Chem Rev 103:4131–4146

2. Akazome M, Kondo T, Watanabe Y (1992) Novel synthesis of indoles via palladium-catalyzed reductive N-heterocyclization of ortho-nitrostyrene derivatives. Chem Lett 21:769–772

3. Alessio E, Mestroni G (1984) Catalytic synthesis of aromatic urethanes from nitroaromatic compounds and carbon monoxide, using palladium + 1,10-phenanthroline derivatives as catalyst precursors. J Mol Catal 26:337–340

4. Alessio E, Mestroni G (1985) Catalytic reductive carbonylation of aromatic nitro compounds to urethanes promoted by supported palladium activated with 1,10-phenanthroline derivatives. J Organomet Chem 291:117–127

5. Alper H, Paik H-N (1978) Influence of carbon monoxide on phase transfer catalyzed reactions of nitro compounds with triirondodecacarbonyl. Nouv J Chim 2:245–247

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