Anionic Ring-Opening Polymerization of 1,2,3,4-Tetramethyl-1,2,3,4-tetraphenylcyclotetrasilane

DOI: 10.1021/ja00003a050

Source and publish data:

Journal of the American Chemical Society p. 1046 - 1047 (1991)

Update date:2022-07-29

Topics:

Authors:

Cypryk, Marek

Gupta, Yogendra

Matyjaszewski, Krzysztof

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

Article abstract of DOI:10.1021/ja00003a050

Full text of DOI:10.1021/ja00003a050

Products guided by the article

Product name:1,2,3,4-tetramethyl-1,2,3,4-tetraphenylcyclotetrasilane

Cas No:120575-00-0

R&D Labs maybe for 120575-00-0

Jiangsu Institute of Ecomones Co., Ltd

website:http://www.jsmone.com

Contact:+86-519-82821700

Address:95 Huanyuan N. Road, Jintan, Jiangsu, China
Yueyang Hudex Pharmaceuticals Ltd.

Contact:0730-8748800

Address:Wujiang Bridge，Yueyang Economy & Technology Development Zone
Aecochem Corp.

website:http://www.aecochemical.com

Contact:+86-592 599 8717

Address:No 611 Sishui Road,Huli
Suzhou Ryan Pharmachem Technology Co.,Ltd

Contact:+86-0512-68780025

Address:B-301,No.2 Taishan Road,Suzhou New District,Jiangsu,P.R. China
SPRING CHEMICAL INDUSTRY CO.,LTD

Contact:86-187-66672125

Address:linchi industry park.zouping

Relevant to this article

Synthesis of nitrogen heterocycle-fused 1,2,4-benzothiadiazine-1,1-dioxide, quinazolinone, and pyrrolidinone derivatives with a guanidine joint via sequential aza-Wittig reaction/intramolecular NH-addition cyclization/nucleophilic substitution ring closur

Doi:10.1016/j.tet.2009.11.064
(2010)
A new fluorescent chemodosimeter for Hg²⁺: Selectivity, sensitivity, and resistance to Cys and GSH

Doi:10.1021/ol902590g
(2010)
One pot synthesis and SAR of some novel 3-substituted 5,6-diphenyl-1,2,4-triazines as antifungal agents

Doi:10.1016/j.bmcl.2009.11.048
(2010)
Model systems for the investigation of the Opsin shift in Bacteriorhodopsin

Doi:10.1021/jp904132f
(2010)
Exploring SAR features in diverse library of 4-cyanomethyl-pyrazole-3-carboxamides suitable for further elaborations as CB1 antagonists

Doi:10.1016/j.bmcl.2009.11.047
(2010)
Synthesis of high enantiopurity N-protected α-amino ketones by thiol ester-organostannane cross-coupling using pH-neutral conditions

Doi:10.1021/ol8018456
(2008)

Article Doi