(±)Trans-2-aminocyclohexanesulfonic acid and (±)trans-2-aminocyclopentanesulfonic acid were prepared respectively from cyclohexene and cyclopentene by sulfur monochloride addition, followed by oxidation to 2-chlorosulfonic acid and substitution of chlorine.
References
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MarvelC.S., and BaileyC. F.Taurine. Org. Synth. Coll. Vol. II, Wiley, New York, 1943, pp. 563.
2.
For some examples see: (a) HigashiuraK., MorinoH., MatsuuraH., ToyomakiY., and IenagaK., J. Chem. Soc., Perkin Trans1989, 1, 1479
3.
GudeM., PiarulliU., PotenzaD., SalomonB., and GennariC., Tetrahedron Lett., 1996, 37, 8589 c) D. Braghiroli, R. Avallone and M. Di Bella, Tetrahedron: Asymmetry, 1997, 8, 2209.
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AndresenB.D., DavisF. T., TaskesP. P., and KingC. E., J. Labelled Compd. Radiopharm., 1978, 15, 731.
5.
(a) BroussalianG.L., U.S. Patent, 3,337,457 (1967)
