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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Synthesis of the beta 2 agonist (R)-salmeterol using a sequence of supported reagents and scavenging agents.

[formula: see text] The enantioselective synthesis of (R)-salmeterol has been achieved by using a sequence of supported reagents and sequestering agents. The saligenin core was installed by a regiospecific alkylation and a chiral auxilliary approach was employed to introduce the desired stereochemistry via a diastereoselective reduction.[1]

References

  1. Synthesis of the beta 2 agonist (R)-salmeterol using a sequence of supported reagents and scavenging agents. Bream, R.N., Ley, S.V., Procopiou, P.A. Org. Lett. (2002) [Pubmed]
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