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  Synthesis of novel tricyclic and tetracyclic sultone scaffolds via intramolecular 1,3-dipolar cycloaddition reactions.

Ghandi, M., Taheri, A., Bozcheloei, A. H., Abbasi, A., & Kia, R. (2012). Synthesis of novel tricyclic and tetracyclic sultone scaffolds via intramolecular 1,3-dipolar cycloaddition reactions. Tetrahedron, 68(18), 3641-3648. doi:10.1016/j.tet.2012.02.053.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-002C-2479-3 Version Permalink: http://hdl.handle.net/11858/00-001M-0000-002C-247D-C
Genre: Journal Article

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 Creators:
Ghandi, M., Author
Taheri, A., Author
Bozcheloei, A. H., Author
Abbasi, A., Author
Kia, R.1, Author              
Affiliations:
1Research Group of Structural Dynamics of (Bio)Chemical Systems, MPI for Biophysical Chemistry, Max Planck Society, ou_578564              

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 Abstract: The initially prepared 2-formylphenyl-(E)-2-phenylethenesulfonates from the condensation of (E)-2-phenylethenesulfonyl chloride with 2-hydroxybenzaldehyde derivatives underwent intramolecular [3+2] cycloaddition with methyl or phenylhydroxylamine, sarcosine, and l-proline, affording the corresponding novel isoxazolidine, pyrrolidine and pyrrolizidine-annulated γ,δ-benzo-δ-sultones, respectively, in good yields. Unambiguous assignment of the molecular structures was carried out by single-crystal X-ray diffraction.

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Language(s): eng - English
 Dates: 2012-05-06
 Publication Status: Published in print
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 Rev. Method: Peer
 Identifiers: DOI: 10.1016/j.tet.2012.02.053
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Title: Tetrahedron
Source Genre: Journal
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Pages: - Volume / Issue: 68 (18) Sequence Number: - Start / End Page: 3641 - 3648 Identifier: -