Difference between revisions of "Birman's synthesis of sceptrin"
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# Birman, V. B.; Jiang, X.-T., "Synthesis of Sceptrin Alkaloids," ''Org. Lett.'' '''2004''' ''6''(14); 2369-2371. DOI: [http://pubs3.acs.org/acs/journals/doilookup?in_doi=10.1021/ol049283g 10.1021/ol049283g] | # Birman, V. B.; Jiang, X.-T., "Synthesis of Sceptrin Alkaloids," ''Org. Lett.'' '''2004''' ''6''(14); 2369-2371. DOI: [http://pubs3.acs.org/acs/journals/doilookup?in_doi=10.1021/ol049283g 10.1021/ol049283g] | ||
# Baran, P. S.; Zografos, A. L.; O'Malley, D. P. "Short Total Synthesis of (±)-Sceptrin" ''J. Am. Chem. Soc.'' '''2004''' ''126''(12); 3726-3727. DOI: [http://pubs3.acs.org/acs/journals/doilookup?in_doi=10.1021/ja049648s 10.1021/ja049648s] | # Baran, P. S.; Zografos, A. L.; O'Malley, D. P. "Short Total Synthesis of (±)-Sceptrin" ''J. Am. Chem. Soc.'' '''2004''' ''126''(12); 3726-3727. DOI: [http://pubs3.acs.org/acs/journals/doilookup?in_doi=10.1021/ja049648s 10.1021/ja049648s] | ||
| − | #Walker, R.P.; Faulkner, D.J.; et al.'' J.Am Chem. Soc''. '''1981''', ''103'', 6772 | + | #Walker, R.P.; Faulkner, D.J.; et al.'' J. Am Chem. Soc''. '''1981''', ''103'', 6772 |
[[Category:Chemistry 444 pages]] | [[Category:Chemistry 444 pages]] | ||
[[Category:Total syntheses]] | [[Category:Total syntheses]] | ||
Revision as of 11:13, 20 April 2007
Contents
Background
Sceptrin is a useful naturally occurring product. found Agelas sceptrum, which is a sponge that inhabits the Glover Reef in Belize. The chemical has anti-bacterial, antiviral, and anti-histaminic properties. Sceptrin also has anti-muscarinic properties. The term muscarinic is derived from Muscarine, which is an alkaloid poison found in certain fungi.
Retrosynthesis
File:Synthesis of Sceptrin IV.jpg
Synthesis of Starting compound
File:Synthesis of Sceptrin III.jpg
Synthesis of Sceptrin (2nd Generation)
File:Synthesis of Sceptrin.jpg
File:Synthesis of Sceptrin II.jpg
Inside the synthesis
The starting four member ring is made via a 2+2 addition in the presence of UV light. In step 3 of the synthesis, the KOH/MeOH changed the orientation of carbon atom in the first position from cis to trans. Guanidine was added in DMF to convert the bromoacetyl groups into imidizole rings. The addition of PPh3 in NH3 fosters the change of the azides into amines
Conclusions
This synthesis is enantioselective, it creates a racemic mixture of sceptrin. It should also be noted that the compound is stereoselective. An interesting feature of this compound lies in the fact that the central ring is a cyclobutane ring, which in usual circumstances is not very stable due to ring strain. The overall synthesis of sceptrin is convergent.
References
- Birman, V. B.; Jiang, X.-T., "Synthesis of Sceptrin Alkaloids," Org. Lett. 2004 6(14); 2369-2371. DOI: 10.1021/ol049283g
- Baran, P. S.; Zografos, A. L.; O'Malley, D. P. "Short Total Synthesis of (±)-Sceptrin" J. Am. Chem. Soc. 2004 126(12); 3726-3727. DOI: 10.1021/ja049648s
- Walker, R.P.; Faulkner, D.J.; et al. J. Am Chem. Soc. 1981, 103, 6772
