Formation of hydridocobalt(III) phthalocyanine by reaction of cobalt(II) phthalocyanines with sodium borohydride and its reactions with antioxidant isoflavones

作者: Poonam , Pratibha Kumari , Ritika Nagpal , Shive M. S. Chauhan

DOI: 10.1039/C1NJ20582J

关键词:

摘要: The reduction of substituted isoflavones with sodium borohydride catalyzed by cobalt(II) phthalocyanines has been achieved efficiently to yield cis- and trans-isoflavan-4-ols under mild conditions via the formation a hydridocobalt(III) phthalocyanine intermediate. hydroxy react form corresponding phenolate moiety thereby prevent intermediate which inhibits its isoflavan-4-ols.

参考文章(67)
Victor N. Nemykin, Evgeny A. Lukyanets, Synthesis of substituted phthalocyanines Arkivoc. ,vol. 2010, ,(2010) , 10.3998/ARK.5550190.0011.104
Xiu-Ling Wang, Hor-Gil Hur, Je Hyeon Lee, Ki Tae Kim, Su-Il Kim, Enantioselective synthesis of S-equol from dihydrodaidzein by a newly isolated anaerobic human intestinal bacterium. Applied and Environmental Microbiology. ,vol. 71, pp. 214- 219 ,(2005) , 10.1128/AEM.71.1.214-219.2005
Mark J Messina, Legumes and soybeans: overview of their nutritional profiles and health effects The American Journal of Clinical Nutrition. ,vol. 70, ,(1999) , 10.1093/AJCN/70.3.439S
S. M. S. Chauhan, Anil Kumar, K. A. Srinivas, Oxidation of thiols with molecular oxygen catalyzed by cobalt(II) phthalocyanines in ionic liquid Chemical Communications. pp. 2348- 2349 ,(2003) , 10.1039/B305888C
Ying Chen, X. Peter Zhang, Vitamin B12 derivatives as natural asymmetric catalysts: enantioselective cyclopropanation of alkenes. Journal of Organic Chemistry. ,vol. 69, pp. 2431- 2435 ,(2004) , 10.1021/JO049870F
Jun-ichiro Setsune, Yoshihiro Ishimaru, Tohru Moriyama, Teijiro Kitao, Hydrometallation of alkenes and alkynes by the combination of cobalt(II) porphyrins, NaBH4 and oxidizing agents Journal of The Chemical Society, Chemical Communications. pp. 555- 556 ,(1991) , 10.1039/C39910000555
W. Lawson, Œstrogenic activity of some derivatives of isoflaven and isoflavanol J. Chem. Soc.. ,vol. 0, pp. 4448- 4450 ,(1954) , 10.1039/JR9540004448