PHOTOSTIMULATED AND DARK REACTION OF ARYL HALIDES WITH 2- AND 3-PYRIDINETHIOLATES

DOI: 10.1007/BF00962315

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 761 - 765 (1987)

Update date:2022-08-05

Topics:

Authors:

Rybakova, I. A.

Shekhtman, R. I.

Prilezhaeva, E. N.

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

Article abstract of DOI:10.1007/BF00962315

Full text of DOI:10.1007/BF00962315

Products guided by the article

Product name:3-nitrophenyl 2-pyridyl sulfide

Cas No:113984-14-8

R&D Labs maybe for 113984-14-8

Eastar Chemical Corporation

website:http://www.eastarchem.com/

Contact:1-800-898-2436

Address:1215 K Street, STE 1700
Zhejiang Rongkai Chemical Technology Co.,Ltd.

Contact:+86-578-8185786

Address:Shangjiang Industrial Zone,Suichang
BrightGene Bio-Medical Technology Co., Ltd.

website:https://en.bright-gene.com/

Contact:+86-512-62551801

Address:Building C25 - C31, No. 218 Xinghu Road, Suzhou Industrial Park, Suzhou, Jiangsu, China.
Hawks Chemical

Contact:+44 (0)161 367 9441

Address:
Zhejiang Hoshine Silicon Industry Co., Ltd.

Contact:86-573-89179966

Address:Zhapu Town, Pinghu City, Zhejiang, China

Relevant to this article

Stereochemical aspects of the hypophosphorous acid addition to terephthalic schiff bases. Synthesis of new 1,4-phenylene-bis-aminomethane-bis-phosphonous acids

Doi:10.1002/hc.20422
(2008)
Rational tuning of visual cycle modulator pharmacodynamics

Doi:10.1124/jpet.117.240721
(2017)
Synthesis of 2([methyl-5-[(E)-2-aryl-1-ethenyl]-4-isoxazolyl]imino)-1,3- thiazolan-4-ones and their Mannich bases

Doi:10.1080/10426500801967856
(2008)
Substituted terphenyl compounds as the first class of low molecular weight allosteric inhibitors of the luteinizing hormone receptor

Doi:10.1021/jm801561h
(2009)
Isoxazole derivatives as centrally acting muscle relaxants. III. Synthesis and activity of conformationally restricted analogs

Doi:10.1248/cpb.35.3676
(1987)
One-Bond Azo Initiators. Thermal Decomposition of Substituted (Phenylazo)triphenylmethanes

Doi:10.1021/ja00350a040
(1983)

Article Doi