33447-90-4Relevant articles and documents
Asymmetric synthesis of trans-2,5-dimethylpyrrolidine
Zwaagstra,Meetsma,Feringa
, p. 2163 - 2172 (2007/10/02)
A new synthetic route to (2S,5S)-dimethylpyrrolidine 1, which can also be applied to the synthesis of the (2R,5R)-enantiomer, has been developed. The C2-symmetric pyrrolidine can be obtained enantiomerically pure (e.e. ≥ 97%) in 15% overall yield starting from a mixture of isomers of 2,5-hexanediol, via a short reaction sequence using (S)-α-methylbenzylamine as a chiral auxiliary. The crystal and molecular structure of (S)-2'-phenyl-N-ethyl-(2S,5S)-dimethylpyrrolidine picrate 5, showing an antiparallel stacking of the picrate units, is also reported.
Alkylating esters VIII. The action of the isomers of dimethylmyleran on spermatogenesis
Jones,Jones
, p. 178 - 179 (2007/10/18)
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