Unsymmetrically substituted aliphatic diacetylenes

DOI: 10.1016/0040-4039(96)01025-8

Source and publish data:

Tetrahedron Letters p. 5023 - 5026 (1996)

Update date:2022-08-30

Topics:

Authors:

Barbu, Eugen

Tsibouklis, John

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

Article abstract of DOI:10.1016/0040-4039(96)01025-8

A general method for the synthesis of pure samples of unsymmetrically disubstituted diacetylenes of the type CH₃-(CH₂)(n)-C=C=C=C-CH₂-OH (n=2,3,4,5) is described in detail. The materials could be polymerized thermally, in the liquid state.

Full text of DOI:10.1016/0040-4039(96)01025-8

Products guided by the article

Product name:1-Iodo-1-hexyne

Cas No:1119-67-1

R&D Labs maybe for 1119-67-1

Daqing E-shine Chemical Co.,LTD

Contact:0086-024-31285112

Address:Hongweiyuan area, Ranghulu district
RongCheng K&S Chemical Co.,Ltd

Contact:0631-7336369

Address:rongcheng ,shandong province china
Shaanxi King Stone Enterprise Company Limited

Contact:86-29-88353805,13609285751

Address:.209 Keji Road Hi-Tech industrial Develpment Zone .Xian China
Guangxi Shanyun Biochemical Science and Technology Co., Ltd

Contact:+86-0772--6828887

Address:#2 Industrial Park of Luzhai County, Liuzhou, Guangxi, China
SuZhou Ascepion Pharmaceuticals, Inc.(expird)

Contact:0512-86881668

Address:Building C,68Xingqing Road,Suzhou,China.

Relevant to this article

Doi:10.1007/BF00475849
()
Transition metal-free hydrodefluorination of acid fluorides and organofluorines by Ph₃GeH promoted by catalytic[Ph₃C][B(C₆F₅)₄]

Doi:10.1039/c9cc05075b
(2019)
Polyethylene glycol (PEG) promoted hydrodehalogenation of aryl halides

Doi:10.1016/j.tetlet.2017.03.016
(2017)
Hierarchically porous Br?nsted acidic ionic liquid functionalized nitrogen-doped carbons for pyrolysis biofuel upgrading via esterification of acetic acid with high boiling point alcohols

Doi:10.1016/j.apcata.2019.01.021
(2019)
Stepwise Reduction of CO to CH4 on a Triosmium Cluster Face. Preparation and Characterization of Os3(CO)11CH2

Doi:10.1021/ja00395a075
(1981)
Multi-center redox-active system: Amine-amine electronic coupling through a cyclometalated bisruthenium segment

Doi:10.1021/ic400082z
(2013)

Article Doi