Formal Total Synthesis of Manzacidin C Based on Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Imines
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Abstract
An enantioselective formal total synthesis of (+)-manzacidin C is described. A key feature of the synthesis is the construction of two chiral centers via the asymmetric 1,3-dipolar cycloaddition of an azomethine imine to methallyl alcohol by the use of (S,S)-DIPT as a chiral auxiliary. © 2017 American Chemical Society.
Embargo Period 12 months
Journal
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- Journal of Organic Chemistry
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Journal of Organic Chemistry 82 (4), 1969-1976, 2017-02-17
American Chemical Society
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Details 詳細情報について
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- CRID
- 1050564285895888896
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- NII Article ID
- 120006027761
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- NII Book ID
- AA00704100
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- ISSN
- 00223263
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- Web Site
- http://hdl.handle.net/2297/46979
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- Text Lang
- en
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- Article Type
- journal article
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- Data Source
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- IRDB
- CiNii Articles