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The Catalyst-Controlled Regiodivergent Chlorination of Phenols
- Source :
- Organic Letters. 18:5476-5479
- Publication Year :
- 2016
- Publisher :
- American Chemical Society (ACS), 2016.
-
Abstract
- Different catalysts are demonstrated to overcome or augment a substrate's innate regioselectivity. Nagasawa's bis-thiourea catalyst was found to overcome the innate para-selectivity of electrophilic phenol chlorination, yielding ortho-chlorinated phenols that are not readily obtainable via canonical electrophilic chlorinations. Conversely, a phosphine sulfide derived from 2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (BINAP) was found to enhance the innate para-preference of phenol chlorination.
- Subjects :
- chemistry.chemical_classification
Sulfide
010405 organic chemistry
Chemistry
Organic Chemistry
Regioselectivity
010402 general chemistry
01 natural sciences
Biochemistry
0104 chemical sciences
Catalysis
chemistry.chemical_compound
Electrophile
polycyclic compounds
Phenol
Organic chemistry
Phenols
Physical and Theoretical Chemistry
Phosphine
BINAP
Subjects
Details
- ISSN :
- 15237052 and 15237060
- Volume :
- 18
- Database :
- OpenAIRE
- Journal :
- Organic Letters
- Accession number :
- edsair.doi.dedup.....8c657a6f169ae9e8db96e18f24958531
- Full Text :
- https://doi.org/10.1021/acs.orglett.6b02650