Published April 2012
| Version v1
Journal article
Direct palladium-catalyzed C-4 arylation of tri-substituted furans with aryl chlorides: An efficient access to heteroaromatics
- 1. College of Chemistry and Chemical Engineering/Hunan Institute of Engineering, Xiangtan (China)
- 2. Guangdong Univ. of Education, Guangzhou (Korea, Republic of)
Description
A series of functionalized furans were synthesized by way of a palladium -catalyzed coupling reaction of 2,3,5-tri substituted furans with aryl chlorides through C-H bond cleavages at C-4 position. The feature of the reaction was facilitative preparation of furan derivatives with good functional group tolerance. All reactions gave the desired products in moderate to good yields in the presences of BuAd2P and t-BuOK in DMF at 120 .deg. C after 15 h
Additional details
Publishing Information
- Journal Title
- Bulletin of the Korean Chemical Society
- Journal Volume
- 33
- Journal Issue
- 8
- Series
- 42 refs, 2 figs, 3 tabs
- Journal Page Range
- p. 2623-2626
- ISSN
- 0253-2964
INIS
- Country of Publication
- Korea, Republic of
- Country of Input or Organization
- Korea, Republic of
- INIS RN
- 45088460
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- AROMATICS; CHLORIDES; CLEAVAGE; FURANS; PALLADIUM
- Descriptors DEC
- CHLORINE COMPOUNDS; ELEMENTS; HALIDES; HALOGEN COMPOUNDS; HETEROCYCLIC COMPOUNDS; METALS; MICROSTRUCTURE; ORGANIC COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; PLATINUM METALS; TRANSITION ELEMENTS