CONVERSIONS OF α-NITROOLEFINS DURING ELECTRON TRANSFER IN SOLUTION

DOI: 10.1007/BF01557517

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 1433 - 1436 (1987)

Update date:2022-08-05

Topics:

Authors:

Todres, Z. V.

Tsvetkova, T. M.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1007/BF01557517

Full text of DOI:10.1007/BF01557517

Products guided by the article

Product name:Benzene, 1,1',1'',1'''-(1,4-dinitro-1,2,3,4-butanetetrayl)tetrakis-

Cas No:114288-80-1

R&D Labs maybe for 114288-80-1

HANGZHOU ICH BIOFARM CO.,LTD

Contact:+86-571-28186845

Address:Room 1224,Eastcom Mansion,398 Wensan Road,Hangzhou,310013 China
Jiangsu Jiuri Chemical Co.,Ltd.

Contact:+86-519-82118868

Address:Tianwang Town, Jurong City, Jiangsu Province, China
Hangzhou Eastbiopharm Co.,Ltd.

Contact:+86-571-88931780

Address:Hangzhou,China
Taizhou YOJOY Chemical Co., Ltd.

Contact:13857143241

Address:Yangfu Industrial Park, Xianju, Zhejiang, P. R. China
Tianjin Tensing Fine Chemical Research Develop Centre

Contact:86-022-23718576,13032267585

Address:2-2-201,13 Guiyuan road,Huayuan Industry district,Tianjin,china

Relevant to this article

Synthesis and antibacterial activity evaluation of metronidazole-triazole conjugates

Doi:10.1016/j.bmcl.2009.01.037
(2009)
Structure-guided discovery of thiazolidine-2,4-dione derivatives as a novel class of Leishmania major pteridine reductase 1 inhibitors

Doi:10.1016/j.ejmech.2016.07.060
(2016)
Total synthesis and biological mode of action of largazole: A potent class I histone deacetylase inhibitor

Doi:10.1021/ja8033763
(2008)
Substituent effect study on the experimental ¹³C NMR chemical shifts of 3-(substituted phenyl)-3a,4,8,8a-tetrahydro-1,3-dioxepino[5,6-d] [1,2] isoxazoles

Doi:10.1016/j.molstruc.2019.04.121
(2019)
A novel method for the high-pressure-promoted, uncatalyzed aza-Michael reaction of nitrogen heterocycles with enones in water

Doi:10.1055/s-2008-1072594
(2008)
Novel β-lactam antibiotics synthesized by amination of catechols using fungal laccase

Doi:10.1248/cpb.56.902
(2008)

Article Doi