119Sn, 15N, 13C and 1H NMR study of some tri- and di-organotin(IV) 8-quinolinethiolates

DOI: 10.1016/0022-328X(89)87227-4

Source and publish data:

Journal of Organometallic Chemistry p. 327 - 338 (1989)

Update date:2022-07-30

Topics:

Authors:

Lycka, Antonin

Jirman, Josef

Holecek, Jaroslav

Tkac, Ivan

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

Article abstract of DOI:10.1016/0022-328X(89)87227-4

Tin-119, nitrogen-15, carbon-13, and proton NMR spectroscopy has been used to study the structures of the triorganotin(IV) 8-quinolinethiolates R3Sn(txin) and the diorganotin(IV) di(8-quinolinethiolates) R2Sn(txin)2, (txinH=8-quinolinethiol; R=n-butyl, be

Full text of DOI:10.1016/0022-328X(89)87227-4

Products guided by the article

Product name:tribenzyltin(IV) 8-quinolinethiolate

Cas No:126029-99-0

R&D Labs maybe for 126029-99-0

Shandong Jincheng Zhonghua Bio-pharmaceutical Co.,Ltd

Contact:+86-533-5415882

Address:Zichuan Economic Development Zone,Zibo City,Shandong Province,China
Shanghai Massive Chemical Technology Co., Ltd.

website:http://www.massivechem.com/

Contact:+86 21 34943721

Address:Room 435, 4th floor, Building 9, No. 2568 Gudai Road,Minhang District, Shanghai,
ChengduChroma-BiotechCo.,Ltd.

Contact:86-28-61993785

Address:No.70-13-21, North Section, Erhuan
Shanghai Taibao Pharmaceutical Technology Co., Ltd(expird)

Contact:021-52217366

Address:shanghai
Shenyang Xinyihan Chemical Technology Co., Ltd.

Contact:+86-18525026267

Address:362, aigongbeijei street 23 , tiexi district,Shenyang, Liaoning, China

Relevant to this article

Palladium-catalyzed allylic C-OH functionalization for efficient synthesis of functionalized allylsilanes

Doi:10.1021/ja1096732
(2011)
Stereocontrolled synthesis of (±)-debromoaplysin, (±)-aplysin, (±)-debromoaplysinol, (±)-aplysinol, and (±)-isoaplysin

Doi:10.1021/jo00298a022
(1990)
Synthesis and stereochemical assignment of (+)-chamuvarinin

Doi:10.1021/ol1028699
(2011)
Design and synthesis of some new pyrazolo[1,5-a]pyrimidines, pyrazolo[5,1-c]triazines, pyrazolo[3,4-d]pyridazines, and isoxazolo[3,4-d] pyridazines containing the pyrazole moiety

Doi:10.1080/00397911.2011.616639
(2013)
Design, synthesis and structure-activity relationship study of novel pyrazole-based heterocycles as potential antitumor agents

Doi:10.1016/j.ejmech.2010.09.054
(2010)
Progress in carbonylative [2+2+1] cycloaddition: Utilization of a nitrile group as the πa component

Doi:10.1002/anie.201305729
(2013)

Article Doi