Organic Synthesis "On Water"

被引:1376
作者
Chanda, Arani [1 ]
Fokin, Valery V. [1 ]
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
关键词
DIELS-ALDER REACTIONS; AZIDE-ALKYNE CYCLOADDITION; SOLVENT-FREE CONDITIONS; TERMINAL ALKYNES; HIGHLY EFFICIENT; 1,3-DIPOLAR CYCLOADDITIONS; ROOM-TEMPERATURE; TRANSITION-STATE; SELECTIVE SYNTHESES; SUZUKI-MIYAURA;
D O I
10.1021/cr800448q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organic transformations that benefit from being performed on water under the conditions defined by Sharpless and co-workers was studied. The Diels-Alder cycloaddition is a powerful synthetic transformation that has been used prolifically by organic chemists, and the effect of aqueous solvents on this large family of reactions. Rideout and Breslow reported in 1990 that both rate enhancement and excellent selectivity could be achieved for certain Diels-Alder reactions when they were performed in dilute aqueous solutions. Sharpless and co-workers in 2005 demonstrated the on-water effect on the Diels-Alder reaction of trans,trans-2,4- hexadienyl acetate 10 and N-propylmaleimide 11. The 1,3-dipolar cycloaddition reactions of phthalazinium ylides on water, reported by Butler and co-workers, are noteworthy because they involve at least one solid reactant. Freeing water from the stereotypes will propel it to a prominent place in the arsenal of tools of synthetic organic chemists.
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页码:725 / 748
页数:24
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