Research Topics
| Jin-Heng LiSummaryAffiliation: Hunan Normal University Country: China Publications
| Collaborators
|
Detail Information
Publications
Reusable copper-catalyzed cross-coupling reactions of aryl halides with organotins in inexpensive ionic liquidsJin Heng Li
Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research Ministry of Education, College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081, China
J Org Chem 71:7488-90. 2006..It is noteworthy that the Cu2O/P(o-tol)3/TBAB system can be recovered and reused at least three times without any loss of catalytic activity among the reactions of aryl iodides and activated aryl bromides...
2-aminopyrimidine-4,6-diol as an efficient ligand for solvent-free copper-catalyzed N-arylations of imidazoles with aryl and heteroaryl halidesYe-Xiang Xie
Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research (Ministry of Education, College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081, China
J Org Chem 71:8324-7. 2006..Noteworthy is that the reaction is conducted under solvent-free conditions...
CuI-catalyzed suzuki-miyaura and sonogashira cross-coupling reactions using DABCO as ligandJin Heng Li
Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research Ministry of Education, College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081, China
J Org Chem 72:2053-7. 2007..A variety of aryl halides and vinyl halides including activated aryl chlorides underwent the coupling with terminal alkynes in moderate to excellent yields...
Electrophilic ipso-iodocyclization of N-(4-methylphenyl)propiolamides: selective synthesis of 8-methyleneazaspiro[4,5]trienesQuan Fu Yu
Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research Ministry of Education, College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081, China
J Org Chem 73:3658-61. 2008..In the presence of ICl or I 2, 8-methylene-1-azaspiro[4,5]trienes were selectively prepared from the electrophilic ipso-iodocyclization of N-(4-methylphenyl)propiolamides in moderate to good yields...
Reusable Cu2O/PPh3/TBAB system for the cross-couplings of aryl halides and heteroaryl halides with terminal alkynesBo Xiao Tang
Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research Ministry of Education, College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081, China
J Org Chem 72:6294-7. 2007..Noteworthy is that the Cu2O/PPh3/TBAB system can be recovered and reused several times without loss of any activities...
Palladium-catalyzed C-H functionalization of N-arylpropiolamides with aryliodonium salts: selective synthesis of 3-(1-arylmethylene)oxindolesShi Tang
Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research Ministry of Education, Hunan Normal University, Changsha 410081, China
J Org Chem 73:5476-80. 2008..It is noteworthy that the reaction can be conducted providing moderate yields even without bases. The mechanism of the reaction was also discussed...
Cycloaddition of arynes with iodonium ylides: a mild and general route for the synthesis of benzofuran derivativesXiao Cheng Huang
Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research Ministry of Education, Hunan Normal University, Changsha, China
Org Lett 10:1525-8. 2008..In the presence of CsF, ortho-silyl aryltriflates were reacted with iodonium ylides smoothly at room temperature in moderate to good yields...
Copper/silver-cocatalyzed Conia-ene reaction of linear beta-alkynic beta-ketoestersChen liang Deng
Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research Ministry of Education, Hunan Normal University, Changsha 410081, China
Org Lett 9:5111-4. 2007..In the presence of (CuOTf)2.C6H6 and AgSbF6 (or AgOAc), a variety of the linear beta-alkynic beta-ketoesters selectively underwent the Conia-ene intramolecular reaction in moderate to good yields...
Selective synthesis of spiro[4,5]trienyl acetates via an intramolecular electrophilic ipso-iodocyclization processBo Xiao Tang
Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research, Hunan Normal University, Changsha, China
Org Lett 10:1063-6. 2008....
Palladium-catalyzed carbonylative annulation reaction of 2-(1-alkynyl)benzenamines: selective synthesis of 3-(halomethylene)indolin-2-onesShi Tang
Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100101, China
Org Lett 9:3413-6. 2007..In the presence of PdX2 and CuX2, 3-(halomethylene)indolin-2-ones were selectively obtained from the carbonylative annulations of 2-(1-alkynyl)benzenamines with CO in moderate to good yields...
Synthesis of (2-oxoindolin-3-ylidene)methyl acetates involving a C-H functionalization processShi Tang
College of Chemistry and Materials Science, Wenzhou University, Wenzhou, China
Org Lett 10:1875-8. 2008....
