NOVEL POLYHYDRONAPHTHALENIC STRUCTURES

DOI: 10.1016/S0040-4039(01)90281-3

Source and publish data:

Tetrahedron Letters p. 1227 - 1230 (1981)

Update date:2022-08-17

Topics:

Authors:

Laguerre, Michel

Dunogues, Jacques

Calas, Raymond

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

Article abstract of DOI:10.1016/S0040-4039(01)90281-3

Novel 1,7-dihydro- or 1,2,6,7-tetrahydronaphthalene derivatives were obtained from naphthalene through a polysilylation/oxidation process as well as 1,4,6,7-tetrakis(trimethylsilyl)naphthalene, a regiospecific precursor of 1,4,6,7-tetrafunctional naphthalenes.

Full text of DOI:10.1016/S0040-4039(01)90281-3

Products guided by the article

Product name:1,2,3,4-Tetrahydronaphthalene

Cas No:119-64-2

R&D Labs maybe for 119-64-2

Synochem Ingredients Corp., Ltd.

Contact:+86-512-5636 2180

Address:Zhangjiagang Free Trade Zone
Changzhou Xuanming Chemical Co., Ltd.

Contact:86 0519 85525329

Address:China Town, Xinbei, Changzhou, Jiangsu Room 6019
KODI CHEMICAL CO., LTD

Contact:021

Address:Pudong
SICHUAN ZHONGBANG NEW MATERIAL CO., LTD

website:http://www.zhongbangst.com

Contact:86-830-2585019

Address:sichuan,china
ShangHai Ruiyi Medical Technology Co.,Ltd.

Contact:+86-21-54718086

Address:No951 Jianchuan RD，Minhang District

Relevant to this article

Doi:10.1021/ja01287a008
(1937)
Surface Chemistry of Perfluoroether: A Study of the Reaction Mechanism of (C2F5)2O with an Al2O3 Surface by FTIR Spectroscopy

Doi:10.1021/j100049a022
(1995)
DNA photocleavage by a cationic BODIPY dye through both singlet oxygen and hydroxyl radical: New insight into the photodynamic mechanism of BODIPYs

Doi:10.1002/cphc.201200224
(2012)
Doi:10.1039/TF9656102122
(1965)
Oligomerization mechanism of tea catechins during tea roasting

Doi:10.1016/j.foodchem.2019.01.163
(2019)
Microwave-enhanced catalyst-free aminolysis of epoxides with anilines in aqueous phase: Efficient synthesis of β-amino secondary alcohols

Doi:10.3184/174751911X13237015498335
(2011)

Article Doi