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[3 + 2]-Cycloaddition of Nonstabilized Azomethine Ylides. 10. An Efficient Strategy for the Construction of x -Azatricyclo[ m . n .0.0 a , b ]alkanes by Intramolecular Cycloaddition of Cyclic Azomethine Ylide †

✍ Scribed by Pandey, Ganesh; Sahoo, Akhila K.; Bagul, Trusar D.

Book ID: 120379027
Publisher: American Chemical Society
Year: 2000
Tongue: English
Weight: 39 KB
Volume: 2
Category: Article
ISSN: 1523-7060
DOI: 10.1021/ol006070s

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[3+2]-Cycloaddition of nonstabilized azomethine ylides, part 9: A general approach for the construction of X-azabicyclo[m.2.1]alkanes in optically pure form by asymmetric 1,3-dipolar cycloaddition reactions

✍ Ganesh Pandey; Joydev K. Laha; A.K. Mohanakrishnan 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 211 KB

## A general strategy for the construction of X-azabicyclo[m.2.1]alkane frameworks in optically pure form is reported by the asymmetric [3+2]-cycloaddition reaction of cyclic azomethine ylides with Oppolzer's acryloyl camphor sultam.