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Tetraallyltin

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For Research Use Only | Not For Clinical Use
CATAP7393433
CAS7393-43-3
Structure
MDL NumberMFCD00008637
Molecular Weight283.00
EC Number230-987-5
InChI KeyXJPKDRJZNZMJQM-UHFFFAOYSA-N
REAXYS Number3536269
Description97%
Density1.179 g/mL at 25 °C (lit.)
Assay97%
BP69-70 °C/1.5 mmHg (lit.)
Linear Formula(H2C=CHCH2)4Sn
Refractive Indexn20/D 1.539 (lit.)
Size5G, 25G
1

Allylation of Carbonyl Compounds Bearing a Hydroxyl Group by Tetraallyltin: Highly Stereoselective Allylation in a Chelation-Controlled Manner

Makoto Yasuda, Tatsuya Fujibayashi, Akio Baba

J Org Chem. 1998 Sep 4;63(18):6401-6404.

PMID: 11672278

1

Catalytic Asymmetric Conjugate Allylation of Coumarins

Yulong Kuang, Xiaohua Liu, Lu Chang, Min Wang, Lili Lin, Xiaoming Feng

Org Lett. 2011 Aug 5;13(15):3814-7.

PMID: 21688863

1

Mechanochemically Driven Transformations in Organotin Chemistry: Stereochemical Rearrangement, Redox Behavior, and Dispersion-Stabilized Complexes

Ross F Koby, Timothy P Hanusa, Nathan D Schley

J Am Chem Soc. 2018 Nov 21;140(46):15934-15942.

PMID: 30366498

1

Synthesis and Structure of Air-Stable Lewis Acidic Binuclear Complex of Zirconocene Pentafluorophenylsulfonate and Its Catalytic Application in the Allylation of Carbonyl Compounds With Tetraallyltin

Renhua Qiu, Xinhua Xu, Yinhui Li, Guoping Zhang, Lingling Shao, Delie An, Shuangfeng Yin

Chem Commun (Camb). 2009 Apr 7;(13):1679-81.

PMID: 19294260

1

Synthesis and Structure of Organobismuth Chlorides and Triflates Containing (C,E)-Chelating Ligands (E=O, S) and Their Catalytic Application in the Allylation of Aldehydes With Tetraallyltin

Nianyuan Tan, Yi Chen, Yongbo Zhou, Chak-Tong Au, Shuang-Feng Yin

Chempluschem. 2013 Nov;78(11):1363-1369.

PMID: 31986647

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