Aggarwal et al. have reported an asymmetric synthesis using the sulfur ylides generated in situ by treating the sulfonium salts 3 and 4 prepared from (1R,4R,5R)-4,7,7-trimethyl-6-thiabicyclo[3.2.1]octane (1), with bases. According to their results, the reactions of 3 with aldehydes and imines afford the corresponding chiral oxiranes and aziridines, respectively, in high yields with diastereo- and enantioselectivities.1) On the other hand, the reactions of 4 with aldehydes also give excellent yields of the corresponding α,β-unsaturated oxiranes with perfect stereoselectivities.1) Moreover, this methodology was also successfully applied to the total synthesis of alkaloids, such as quinine.1)
Thus, 1 and 2 are useful chiral auxiliaries applicable to the synthesis of various oxiranes and aziridines via sulfur ylides.
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Useful Chiral Auxiliaries for the Synthesis of Chiral Oxiranes
No.149(December 2012)
References
- 1)Practical and highly selective sulfur ylide mediated asymmetric epoxidations and aziridinations using an inexpensive, readily available chiral sulfide
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