REARRANGEMENTS OF SODIUM SALTS OF ORGANIC SILANOLS

DOI: 10.1007/BF01157371

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 225 - 226 (1985)

Update date:2022-08-03

Topics:

Authors:

Zhdanov, A. A.

Levitskii, M. M.

Dubchak, I. L.

Shilkloper, O. Yu.

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

Article abstract of DOI:10.1007/BF01157371

Full text of DOI:10.1007/BF01157371

Products guided by the article

Product name:disodium 1,1,3,3-tetramethyldisiloxane-1,3-diolate

Cas No:17325-21-2

R&D Labs maybe for 17325-21-2

Luoyang Aoda chemical Co.,Ltd.

Contact:+86-379-67518785 67516588

Address:MiaoWan industry district,YanShi City,Henan,China
SuZhou LaiTeou

Contact:+86-0512-88957371

Address:shanghai
puyang hongda shengdao new material co.,ltd.

Contact:+86-393- 4896278

Address:No.29 East Zhongyuan Road
Jingzhou TianHe Sci&Tech Chemical Co., Ltd.

Contact:86-716-8331612

Address:Jiangjin Road, #18, High-grade technology industries development district, Jingzhou city, Hubei province
ALPHA PHARMACEUTICAL CO，LTD JIANGSU

Contact:+86-527-84829968,+86-527-84829998

Address:suqian city

Relevant to this article

Olefin ring closing metathesis and hydrosilylation reaction in aqueous medium by grubbs second generation ruthenium catalyst

Doi:10.1021/jo801330c
(2008)
Ureido-based peptidomimetic inhibitors of herpes simplex virus ribonucleotide reductase: An investigation of inhibitor bioactive conformation

Doi:10.1021/jm950825x
(1996)
Doi:10.1246/bcsj.27.53
(1954)
Genesis of Tetrathiooxalate-like C2S4 and C2Se4 Units. A Multiform Experimental Study and the Relevant Theoretical Implications for the Role of Transition-Metal Fragments

Doi:10.1021/ja00235a029
(1987)
BORON TRICHLORIDE CATALYZED ORTHO CARBONYLATION OF PHENOLS: SYNTHESIS OF 2-HYDROXY-ARYL-CARBOXYAMIDES AND -KETONES.

Doi:10.1016/S0040-4020(01)87495-0
(1986)
Synthesis and in vitro pharmacology of new 1,4-dihydropyridines. 1. 2-(ω-Aminoalkylthiomethyl)-1,4-dihydropyridines as potent calcium channel blockers

Doi:10.1016/0223-5234(93)90038-G
(1993)

Article Doi