Generation of Allylic and Related Organozirconiums Through A Highly Effective Zirconium-β-Alkoxide Elimination Reaction

DOI: 10.1016/0040-4020(94)01137-O

Source and publish data:

Tetrahedron p. 4507 - 4518 (1995)

Update date:2022-08-05

Topics:

Authors:

Ito, Hisanaka

Nakamura, Takanori

Taguchi, Takeo

Hanzawa, Yuji

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

Article abstract of DOI:10.1016/0040-4020(94)01137-O

Reactions and characterization of allylic and related zirconium reaegnts (allenic and γ-alkoxyallylic zirconiums) generated by treatment of allylic and/or propargylic ethers with a zirconocene-butene complex ("Cp2Zr") are described.

Full text of DOI:10.1016/0040-4020(94)01137-O

Products guided by the article

Product name:Benzeneethanol, a-phenyl-b-1-propenylidene-

Cas No:81435-47-4

R&D Labs maybe for 81435-47-4

Dongtai Xinyuan Chemical Co., Ltd.

Contact:+86-21-56733000

Address:404F, 99Nong No.117 Zhongtan Rd. Shanghai
chemonlinephramacistdepot

Contact:86-607-68073220

Address:1 ave na road jiahua st
KODI CHEMICAL CO., LTD

Contact:021

Address:Pudong
Anhui Xinyuan Technology Co.,Ltd

Contact:0086-559-3515800

Address:No.16 Zijin Rd, Circular Economic Zone, Huizhou District, Huangshan Anhui China
Anhui Redstar Pharmaceutical Corp., Ltd

Contact:+86-563-5120837

Address:Jingxian Industrial Development Zone, Anhui , China

Relevant to this article

New method for the synthesis of indolo [3,2-b] indole derivatives

Doi:10.1007/BF00512959
(1982)
Interproton Coupling over Five Bonds ⁵J(H-C_α-C(O)-N-C_α-H) in the Peptide Moiety: The Importance of Specific Association Effects

Doi:10.1021/ja00376a009
(1982)
AN APPROACH TO REGIOSELECTIVE ALKYLATION OF ALKYL β-D-GALACTOPYRANOSIDES THROUGH (TRIALKYLSTANNYL)ATION

Doi:10.1016/S0008-6215(00)81006-X
(1982)
Electrochemical Induced Regio- and Stereoselective Difunctionalization of Alkynes: The Synthesis of (E)-β-Iodovinyl Sulfones

Doi:10.1002/ejoc.202100505
(2021)
A facile strategy to achieve fully bio-based epoxy thermosets from eugenol

Doi:10.1039/c9gc01184f
(2019)
Synthesis of 16-aryl-15-oxadispiro[5.1.5.3]hexadecane-7,14-diones by reformatsky reaction

Doi:10.1134/S1070428015040089
(2015)

Article Doi