STUDIES ON POSITIONAL PROTECTIVE GROUPS. VI. THE PREPARATION OF 2,6-DICHLORO- AND 2,6-DIBROMOPHENOL FROM THE CORRESPONDING TETRAHALOGEN SUBSTITUTED BISPHENOL A-Reference-Cited by-同舟云学术

STUDIES ON POSITIONAL PROTECTIVE GROUPS. VI. THE PREPARATION OF 2,6-DICHLORO- AND 2,6-DIBROMOPHENOL FROM THE CORRESPONDING TETRAHALOGEN SUBSTITUTED BISPHENOL A

Published:1975-08 Issue:4 Volume:7 Page:189-192
ISSN:0030-4948
Container-title:Organic Preparations and Procedures International
language:en
Short-container-title:Organic Preparations and Procedures International

Author:

Tashiro M.,Watanabe H.,Oe K.

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00304947509355144

Reference5 articles.

1. STUDIES ON POSITIONAL PROTECTIVE GROUPS. V. A NEW PREPARATIVE METHOD FOR 4,4′-DIHYDROXY DIPHENYLMETHANES WITH THE CHLORO OR BROMO GROUPS AS A PROTECTIVE GROUP

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1. Trifluoromethanesulphonic acid catalysed transalkylation between tetrabromobisphenol-a and toluene for the production of 2,6-dibromophenol;Journal of Chemical Technology & Biotechnology;2007-04-24

2. A New Reaction of Bisphenol A and Preparation of Polysubstituted 9,9-Dimethylxanthenes;The Journal of Organic Chemistry;1997-02-01

3. One or More CH Bond(s) Formed by Substitution: Reduction of Carbon–Nitrogen, –Phosphorus, –Arsenic, –Antimony, –Bismuth, –Carbon, –Silicon, –Germanium, –Boron, and –Metal Bonds;Comprehensive Organic Functional Group Transformations;1995

4. References to Volume 1;Comprehensive Organic Functional Group Transformations;1995

5. SELECTIVE ELECTROPHILIC AROMATIC SUBSTITUTIONSVIAPOSITIONAL PROTECTIVE GROUPS: A REVIEW;Organic Preparations and Procedures International;1976-04