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Journal of Zhejiang University SCIENCE A 2000 Vol.1 No.2 P.184-185

http://doi.org/10.1631/jzus.2000.0184


STUDY ON STABLE NITROXYLS(II):SYNTHESIS OF SPIN LABELED PHENOXYACETATES AS POTENTIAL AUXINS


Author(s):  MA Cheng(

Affiliation(s):  Dept.of Chemistry, Yuquan Campus of Zhejiang University, Hangzhou 310027, China

Corresponding email(s): 

Key Words:  auxins, nitroxyls, phase-transfer catalyses, characterization


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MA Cheng(. STUDY ON STABLE NITROXYLS(II):SYNTHESIS OF SPIN LABELED PHENOXYACETATES AS POTENTIAL AUXINS[J]. Journal of Zhejiang University Science A, 2000, 1(2): 184-185.

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Abstract: 
The syntheses and characterization of six new spin labeled phenoxyacetates as potential auxins are described.

Darkslateblue:Affiliate; Royal Blue:Author; Turquoise:Article

Reference

[1]Chen Yaozu, Zhang Changjiu, and Tian Xuan, 1987. Spin labeled antitumor derivatives of podophyllotoixn. Scientia Sinica, Series B 30(10): 1070.

[2]Fawcett, C.H., Spencer, D.M. and Wain R.L., 1957. Investigation fungicides and systemic fungicides. Ann. Appl. Biol. 45: 158.

[3]Goffman, T., Cuscela, D., Glass J., et al., 1992. Topical application of nitroxide protects radiation-induced alopecia in guinea pigs. Int. J. Radiat. Oncol. Bio. Phys. 22(4): 803-806.

[4]Hsia, J.C., Piette, L.H., 1969. Spin labeling as a general method in studying antibody active site. Arch. Biochem.Biophys. 129(1): 296-307.

[5]Kocherginsky, N. and Swartz H.M., 1995. In Nitroxide Spin Labels, Reaction in biology and chemistry, CRC Press,New York, p.175-197.

[6]Li Zhengming, 1993. The status and development of pesticide chemistry research. Chinese J. Appl. Chem. 10(5): 14.

[7]Rozantsev, E.G., 1963.Reactions of a new organic radical which do not affect the free valence. Izv.Akad. Nauk SSSR, Ser. Khim. 9:1669-1672.

[8]Sankarapandi, S., Woodford, J.K., Krstenansky, J.L., et al., 1994.Binding of fluoresent and spin-labeled C-terminal hirudin analogs to thrombin. J. Med. Chem. 37: 3855-3858.

[9]Wang Junzhi, Tian Xuan, Tsumura, H., et al., 1993. Antitumor activity of a new low immunosuppressive derivative of podophyllotoixn(GP-11) and its mechanisms. Anti-cancer Drug Design, 8: 193.

[10]Wang Yanguang, Tian Xuan, Li Jinxin, et al., 1992. Synthesis of spin labeled anticancer derivatives of 5-fluorouracil. Chem. J. Chin. Univ. 12: 1561.

[11]Wang Yanguang, Pan Jianlin, Shi Jianfeng, et al., 1997. New spin labeled analogs of podopphyllotoixn as potetial antitumor agents. Life Sciences, 61: 537-542.

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