Scholarly article on chloro-pent-1-en-t-yl-mercury 115476-30-7 from Journal of Organometallic Chemistry p. 1,4,6

DOI: 10.1016/S0022-328X(00)85115-3

Source and publish data:

Journal of Organometallic Chemistry p. 1,4,6 (1972)

Update date:2022-08-04

Topics:

Authors:

Larock Larock

Brown Brown

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

Article abstract of DOI:10.1016/S0022-328X(00)85115-3

Full text of DOI:10.1016/S0022-328X(00)85115-3

Products guided by the article

Product name:chloro-pent-1-en-t-yl-mercury

Cas No:115476-30-7

R&D Labs maybe for 115476-30-7

Skyrun Industrial Co.,Ltd(expird)

website:http://www.chinaskyrun.com

Contact:0086-576-84610586

Address:Chemical Development Zone
Wuhan Jadechem International Trade Co.,Ltd.

website:http://www.jadechem-intl.com

Contact:+86-27-83527060

Address:Room 502,Building C11,Software new city No.8,Huacheng Avenue,East Lake High-tech development zone,Wuhan,Hubei,China
HANGZHOU ZHONGCHANG SCIENTIFIC CO.,LTD

Contact:+86-571-88932183

Address:Hangzhou
JIEJIE GROUP CO.,LTD.

Contact:+86 021-51698675

Address:1701, Jielong Plaza, No.618 Pingliang Rd, ShangHai,China

Relevant to this article

SYNTHESIS AND MUTAGENIC ACTION OF TETRAHYDROPYRANYL- AND TETRAHYDROTHIOPYRANYL PYRAZOLES AND PYRIMIDINES

Doi:10.1007/BF00768246
(1988)
2-Trifluoroacetylthiophenes, a novel series of potent and selective class II histone deacetylase inhibitors

Doi:10.1016/j.bmcl.2008.02.026
(2008)
Synthesis of Sugar Amino Acids by Triflate Substitution. 2. Free 3- and 4-Amino Acid Deoxyaldopyranoses

Doi:10.1021/jo00252a012
(1988)
Sulfamic acid as a green, reusable catalyst for stepwise, tandem & one-pot solvent-free synthesis of pyrazole derivatives

Doi:10.1016/j.cclet.2017.02.005
(2017)
Synthesis and thermochemical properties of stereoisomeric dihydroxy- and tetrahydroxyalkylammonium salts

Doi:10.1055/s-0028-1088163
(2009)
In Situ Generation of Nitrilimines from Aryldiazonium Salts and Diazo Esters: Synthesis of Fully Substituted Pyrazoles under Room Temperature

Doi:10.1021/acs.orglett.8b00750
(2018)

Article Doi

DOI: 10.1016/S0022-328X(00)85115-3