The detailed mechanism for the reaction of bare iron(I) ions with tert-butyl cyanide and isocyanide in the gas phase

DOI: 10.1021/om00109a040

Source and publish data:

Organometallics p. 1820 - 1822 (1989)

Update date:2022-08-02

Topics:

Authors:

Eller, Karsten

Schwarz, Helmut

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

Article abstract of DOI:10.1021/om00109a040

Experimental, evidence is presented demonstrating that bare Fe⁺ does not insert in the C-X bond of (CH₃)₃C-X (X = CN, NC). Rather, initial "end-on" complexation of the functional group induces cleavage of this bond which i

Full text of DOI:10.1021/om00109a040

Products guided by the article

Product name:CFeN*H⁽¹⁺⁾

Cas No:156885-73-3

R&D Labs maybe for 156885-73-3

Dalian Join King Biochemical Tech. Co., Ltd.

Contact:0411 39216206

Address:814 First State Blvd
shijiazhuang alkay chemicals co..ltd(expird)

Contact:86-311-67692035

Address:2601,juntang building,qiaodong district,shijiazhuang
Global United Biotechnology Inc.

Contact:+86-21-61618568

Address:Room 309, Building 6, NO.135, Jinyu Road, Pudong
Beijing Harmony Chemical Co., Ltd.

Contact:86-010-84956928

Address:Room 207, Jin feng he B building, No 8 Xin Jie Kou Wai Street, Xi Cheng District, Beijing,PRC. 10008
Shangyu Sanhechemicals Co.,LTD.

Contact:86-0571-56696839

Address:Num.2952,Nanhuan Road,Binjiang District,Hangzhou,China

Relevant to this article

4-SYMMETRIC CHIRAL PORPHYRINS">A NEW "5+1" ROUTE ARENES. APPLICATION TO THE FACILE SYNTHESIS OF D₄-SYMMETRIC CHIRAL PORPHYRINS

Doi:10.1016/S0040-4039(00)77145-0
(1994)
Doi:10.1021/ja01603a037
(1956)
Synthetic study of kosinostatin aglycone: Synthesis of BCDE rings using alkoxycarbonylmethylation of diazonaphthoquinone

Doi:10.1016/j.tetlet.2014.01.082
(2014)
Synthesis of Morita–Baylis–Hillman-fluorides using 1,1,2,2-tetrafluoroethyl-N,N-dimethylamine

Doi:10.1016/j.tet.2021.132387
(2021)
Transmembrane anion transport and cytotoxicity of synthetic tambjamine analogs

Doi:10.1039/c3ob42341g
(2014)
Doi:10.1021/jo01267a010
(1968)

Article Doi