期刊
ARKIVOC
卷 -, 期 -, 页码 23-49出版社
ARKAT USA INC
DOI: 10.24820/ark.5550190.p010.416
关键词
1,3-Dipole; azomethine ylide; carbonyl ylide; intramolecular; dipolar cycloaddition; alkaloid synthesis
资金
- National Science Foundation [CHE-1057350]
- Camille and Henry Dreyfus Foundation
As highlighted in this mini review, a growing area of interest in organic synthesis involves the use of substituted azomethine and carbonyl ylides as 1,3-dipoles for the preparation of alkaloidal natural products. Cascade reactions proceeding by an intramolecular 1,3-dipolar cycloaddition of nitrogen and oxygen dipole ylides are of particular interest to the synthetic organic community because of the increase in molecular complexity involved and the high isolated yields. [GRAPHICS] .
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