Weiliang Bao
Hangzhou University
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Publication
Featured researches published by Weiliang Bao.
Synthetic Communications | 1996
Weiliang Bao; Yongmin Zhang; Jingang Wang
Abstract Catalyzed by SmI3 β-diketones and β-ketoesters condense with aldehydes to give benzylidene substituted β-diketones and β-ketoesters at room temperatures in fair yields.
Synthetic Communications | 1996
Weiliang Bao; Yongmin Zhang; Taokai Ying
Abstract Promoted by SmI3 cycloalkanone trimethylsilyl enol ethers were reacted with aldehydes to give α,α′-bis (substituted-benzylidene) cycloalkanones.
Synthetic Communications | 1996
Junquan Wang Yongmin Zhang; Weiliang Bao
Abstract Imines can be readily allylated with samarium/allyl bromide system to afford homoallylamines in satisfactory yields in THF under mild conditions.
Synthetic Communications | 1995
Weiliang Bao; Yongmin Zhang
Abstract Six membered rings of isopropylidene malonate derivatives were opened by aryl thiolate anions and aryl selenolate anions which were produced through reductive cleavage of diaryl disulfides and diaryl diselenides with SmI2, and the substituted propenoic acid selenoaryl and thioaryl esters were synthesized.
Synthetic Communications | 1997
Yunfa Zheng; Weiliang Bao; Yongmin Zhang
Abstract Promoted by indium, allylic and propargyl bromides react with diorganyl diselenides in THF to give allylic and propargyl selenides in moderate to good yields.
Synthetic Communications | 1997
Weiliang Bao; Yongmin Zhang
Abstract Mediated by gallium metal 1-(α-aminoalkyl)benzotriazole reacted with allylic and propargyl bromide to give homoallylic and homopropargyl amines in moderate to good yields.
Tetrahedron Letters | 1996
Taokai Ying; Weiliang Bao; Yongmin Zhang; Weinming Xu
Abstract SmI 2 promoted condensation of α-haloketones with carboxylic acid chlorides or anhydrides leads to 1,3-diketones.
Synthetic Communications | 1995
Weiliang Bao; Yongmin Zhang
Abstract Aryltellurolate ions which were obtained from diaryl ditellurides by reductive cleavage in the aid of SmI2 undergo nucleophilic substitution reaction on aromatic rings and a series of new unsymmetrical diaryl tellurides were synthesized.
Synthetic Communications | 1996
Taokai Ying; Weiliang Bao; Yongmin Zhang
Abstract Promoted by SmI3, α-haloketones were reacted with acid chlorides or acid anhydrides and β-diketones were synthesized via intermediate samarium enolates.
Synthetic Communications | 1994
Weiliang Bao; Yongmin Zhang; Shuangwei Chen
Abstract Arylselenolate Ions which were produced through reductive cleavage of Se-Se bond in diaryl diselenide undergo nucleophilic substitution on aromatic rings and a series of new unsymmetrical diaryl selenides were synthesized.