2-Formylbenzenesulphonyl Chloride as a Reagent for the Protection of Phenols

DOI: 10.1039/c39870000654

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 654 - 656 (1987)

Update date:2022-08-04

Topics:

Authors:

Shashidhar, M. S.

Bhatt, M. Vivekananda

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

Article abstract of DOI:10.1039/c39870000654

2-Formylbenzenesulphonate esters of phenols are rapidly cleaved by alkali leaving carboxylate esters untouched.

Full text of DOI:10.1039/c39870000654

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:Benzenesulfonic acid, 2-formyl-, 3-(acetyloxy)phenyl ester

Cas No:112211-80-0

R&D Labs maybe for 112211-80-0

Shijiazhuang Haitian Amino Acid Co., Ltd.

Contact:+86-311-88908111

Address:Shijiazhuang Hebei province,China
Jining Shengrun Chemical Industry Co., Ltd.

Contact:+86-537-7121666 ,

Address:West Ring Road,Wenshang County Shandong Province
C-LAB Chemievermittlung GmbH

Contact:+49-9398-993127

Address:Untertorstr. 27
LIAOYANG WANRONG CHEMICALS COMPANY LIMITED

Contact:86-419-2390789

Address:XINLI VILLAGE , DONG NINGWEI COUNTY,TAIZIHE DISTRICT, LIAOYANG , LIAONING
Qingzhou Baibang import and export co.,Ltd

Contact:+86-536-3265899

Address:No.338, Tuoshan Road

Relevant to this article

BASISCHE METALLE. XLIV. DARSTELLUNG UND PROTONIERUNG DER KOMPLEXE C5H5Rh(C2R2)PPrⁱ3: ZUR UMWANDLUNG EINER RHODIUM-TOLAN- IN EINE ISOMERE RHODAINDEN-VERBINDUNG

Doi:10.1016/S0022-328X(00)98566-8
(1983)
Gas Phase Negative Ion Chemistry of 6-Oxa-3-sila- and Germabicyclo<3.1.0>hexanes

Doi:10.1246/cl.1987.235
(1987)
The MOF-driven synthesis of supported palladium clusters with catalytic activity for carbene-mediated chemistry

Doi:10.1038/nmat4910
(2017)
Phosphinoyl Radical Initiated Vicinal Cyanophosphinoylation of Alkenes

Doi:10.1021/acs.orglett.7b02621
(2017)
Doi:10.1039/c39790000279
(1979)
Zeolite-catalyzed environmentally friendly tetrahydropyranylation of alcohols and phenols

Doi:10.1081/SCC-200036596
(2004)

Article Doi