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涂永强, Yan Xing Jia, †, Bin Wu, Xin Li, Shi Kuo Ren, Yong Qiang Tu, *, Albert S. C. Chan, ‡, and William Kitching§
Org. Lett., Vol. 3, No 6, 2001,-0001,():
-1年11月30日
The stereocontrolled synthesis of (2S,4R,6R,8S,10S,1
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涂永强, Bao Min Wang, Zhen Lei Song, Chun An Fan, Yong Qiang Tu, *, and Yian Shi†
Org. Lett., Vol. 4, No.3, 2002,-0001,():
-1年11月30日
A new Lewis acid promoted rearrangement reaction of 2,3-aziridino alcohols was discovered, which involved the highly stereoselective construction of a diastereogenic quaternary carbon center and efficient formation of
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涂永强, Lei Shi, Min Wang, Chun-An Fan, Fu-Min Zhang, and Yong-Qiang Tu*
Org. Lett., Vol. 5, No.19, 2003,-0001,():
-1年11月30日
A rapid and direct amination of aryl halides has been developed in good to high yields under microwave irradiation without a transition-metal catalyst. This reaction is a particularly powerful method for the coupling of electron-rich aryl halides with various amines. In some cases, the excellent regioselectivity could be observed, which facilitated the preparation of meta-substituted anilines from ortho- or para-substituted phenylhalides. In addition, a mechanism via the interesting benzyne intermediate has been proposed.
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涂永强, Zhen Lei Song, Bao Min Wang, Yong Qiang Tu, *, Chun An Fan, and Shu Yu Zhang
Org. Lett., Vol. 5, No.13, 2003,-0001,():
-1年11月30日
A short and general approach to the cis-3a-aryloctahydroindole alkaloids has been developed on the basis of a key stereocontrolled ZnBr2-catalyzed rearrangement of 2,3-aziridino alcohols. Two representative members, (
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涂永强, Lei Shi, Yong-Qiang Tu, *, Min Wang, Fu-Min Zhang, and Chun-An Fan
Org. Lett., Vol. 6, No.6, 2004,-0001,():
-1年11月30日
An efficient three-component coupling of aldehyde, alkyne, and amine to generate propargylamines has been effected under microwave irradiation in water using only CuI catalyst without the noble metal cocatalyst. This method has proved to be applicable to a wide range of substrates. In addition, the preliminary experiment using (S)-proline methyl ester as a chiral source demonstrated that it could be developed to be a direct and highly diastereoselective method for construction of chiral propargylamines.
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