Literature DB >> 32336783

Oxidation of N-heterocyclics: A green approach.

Ganarajan Sivasubramanian1, Veembil Ramachandran Parameswaran1.   

Abstract

chemical structure image Environmentally benign oxidation methods satisfy the postulates of green chemistry. Heterocyclic Noxides have applications in synthetic organic chemistry, chemotherapy and agrochemicals. Synthesis of Noxides using green oxidants will be attractive over the conventional methods. The presence of the N-oxide group in the azine ring makes it more subject to electrophilic and nucleophilic attack and substantially expands the synthetic approaches for the modification of nitrogen-containing heterocyclics. That is the reason for the increasing interest in the chemistry of heterocyclic N-oxides. Some reactions adopted for oxidation of N-heterocyclics have been discussed. Stereochemical and spectroscopic aspects have been mentioned. It will be advantageous if anchored catalysts are employed for industrial exploitation. Several physiochemical aspects of various methods have been discussed.
Copyright © 2007 Journal of Heterocyclic Chemistry.

Entities:  

Year:  2009        PMID: 32336783      PMCID: PMC7166534          DOI: 10.1002/jhet.5570440601

Source DB:  PubMed          Journal:  J Heterocycl Chem        ISSN: 0022-152X            Impact factor:   2.193


  13 in total

1.  High oxidation state multiple metal-carbon bonds.

Authors:  Richard R Schrock
Journal:  Chem Rev       Date:  2002-01       Impact factor: 60.622

2.  Palladium-catalyzed enantioselective oxidations of alcohols using molecular oxygen.

Authors:  D R Jensen; J S Pugsley; M S Sigman
Journal:  J Am Chem Soc       Date:  2001-08-01       Impact factor: 15.419

3.  High Turnover Numbers for the Catalytic Selective Epoxidation of Alkenes with 1 atm of Molecular Oxygen We acknowledge T. Hayashi (The University of Tokyo), M. Wada (Nippon Shokubai Co., Ltd.), and Y. Sumita (Nippon Shokubai Co., Ltd.) for their help with experiments. This work was supported in part by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports and Culture of Japan.

Authors:  Yoshiyuki Nishiyama; Yoshinao Nakagawa; Noritaka Mizuno
Journal:  Angew Chem Int Ed Engl       Date:  2001-10-01       Impact factor: 15.336

4.  Reactivity of a titanium dinitrogen complex supported by guanidinate ligands: investigation of solution behavior and a novel rearrangement of guanidinate ligands.

Authors:  S M Mullins; A P Duncan; R G Bergman; J Arnold
Journal:  Inorg Chem       Date:  2001-12-31       Impact factor: 5.165

5.  Molecular sieve catalysts for the regioselective and shape- selective oxyfunctionalization of alkanes in air.

Authors:  J M Thomas; R Raja; G Sankar; R G Bell
Journal:  Acc Chem Res       Date:  2001-03       Impact factor: 22.384

6.  Oxo transfer reactions mediated by bis(dithiolene)tungsten analogues of the active sites of molybdoenzymes in the DMSO reductase family: comparative reactivity of tungsten and molybdenum.

Authors:  K M Sung; R H Holm
Journal:  J Am Chem Soc       Date:  2001-03-07       Impact factor: 15.419

7.  Pd(ii)-hydrotalcite-catalyzed oxidation of alcohols to aldehydes and ketones using atmospheric pressure of air.

Authors:  N Kakiuchi; Y Maeda; T Nishimura; S Uemura
Journal:  J Org Chem       Date:  2001-10-05       Impact factor: 4.354

8.  A new mode of reactivity for pyridine N-oxide: C-H activation with uranium(IV) and thorium(IV) bis(alkyl) complexes.

Authors:  Jaime A Pool; Brian L Scott; Jaqueline L Kiplinger
Journal:  J Am Chem Soc       Date:  2005-02-09       Impact factor: 15.419

9.  A terminal and four-coordinate titanium alkylidene prepared by oxidatively induced alpha-hydrogen abstraction.

Authors:  Falguni Basuli; Brad C Bailey; John Tomaszewski; John C Huffman; Daniel J Mindiola
Journal:  J Am Chem Soc       Date:  2003-05-21       Impact factor: 15.419

10.  Pyridine N-oxide derivatives are inhibitory to the human SARS and feline infectious peritonitis coronavirus in cell culture.

Authors:  Jan Balzarini; Els Keyaerts; Leen Vijgen; Frank Vandermeer; Miguel Stevens; Erik De Clercq; Herman Egberink; Marc Van Ranst
Journal:  J Antimicrob Chemother       Date:  2005-12-30       Impact factor: 5.790

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