⌘+K

Pulse Explore Clubs Researchers Journals

Home Clubs Explore

January 1, 2001Chemical Communications

2-Phenyl-N-tosylazetidine as a formal 1,4 dipole precursor

View Full Paper

Ask AI

Bookmark

Share

Abstract

N-Tosyl-2-phenylazetidine 1 in the presence of BF3·Et2O reacts as a formal 1,4 dipole with various activated or non activated alkenes.

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Ungureanu et al. (2001) studied this question.

synapsesocial.com/papers/6aa6c1ff014c9b816df4fcbc https://doi.org/10.1039/b101168p

View Full Paper

Ask AI

Bookmark

Share

Keep reading

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

1Stereoselective Synthesis of Tetrahydropyrans via a Formal [4 + 2]-Cycloaddition of AllylsilanesOriginal Research · 1999 · 31 citations
2Diastereoselective Reactions of Chiral Allyl and Allenyl Silanes with Activated C:X .pi.-BondsOriginal Research · 1995 · 525 citations
3Allyldimethyltritylsilane. Synthesis of Cyclopentanols, Oxetanes, and Tetrahydrofurans by Reaction with Electron Deficient OlefinsOriginal Research · 1998 · 45 citations
4Structure-Activity Study of Tripeptide Thrombin Inhibitors Using .alpha.-Alkyl Amino Acids and Other Conformationally Constrained Amino Acid SubstitutionsOriginal Research · 1995 · 46 citations