Parallel synthesis and purification using anthracene-tagged substrates.
X Wang, J J Parlow, J A Porco
文献索引：Org. Lett. 2(22) , 3509-12, (2000)
全文：HTML全文
摘要
[reaction: see text] A new strategy for the synthesis and purification of synthetic intermediates is described using anthracene-tagged ester substrates in conjunction with an N-benzylmaleimide resin. Anthracene chemical tags permit use of standard solution-phase reaction conditions and reaction-monitoring techniques.
相关化合物
相关文献：
1996-05-01
[Biochem. Soc. Trans. 24(2) , 313S, (1996)]
Copolymerization of optically active N-(l-menthoxycarbonylmethyl) maleimide with N-phenyl-or N-benzylmaleimide. Kagawa K, et al.
[Polymer 36(5) , 941-48, (1995)]
Microwave-induced One-pot Synthesis of N-carboxyalkyl Maleimides and Phthalimides. Borah N, et al.
[J. Chem. Res. Synop. 5 , 272-3, (1998)]
Asymmetric cycloaddition of anthrone with N-substituted maleimides with C2-chiral pyrrolidines. Tokioka K, et al.
[Tetrahedron Asymmetry 8(1) , 101-7, (1997)]
Iridium-catalyzed double incorporation reaction of N-benzylmaleimide to styrene via ortho-C-H bond activation, initiated by precoordination of the double bond of styrene to iridium. Kiyooka S-I and Takeshita Y.
[Tetrahedron Lett. 46(25) , 4279-82, (2005)]