Concerning the synthesis and enantioselective rearrangements of episulfoxides
Blake, Alexander J.; Cooke, Paul A.; Kendall, Jackie D.; Simpkins, Nigel S.; Westaway, Susan M.; Blake Alexander J.; School of Chemistry, The University of Nottingham; Cooke Paul A.; School of Chemistry, The University of Nottingham; Kendall Jackie D.; School of Chemistry, The University of Nottingham; Simpkins Nigel S.; School of Chemistry, The University of Nottingham; Westaway Susan M.; School of Chemistry, The University of Nottingham
Журнал:
Journal of the Chemical Society, Perkin Transactions 1
Дата:
2000
Аннотация:
A novel synthesis of episulfoxides having the norbornane skeleton is possible by use of a rhodium catalyst to effect SO transfer from trans-stilbene episulfoxide to norbornene or norbornadiene. Analogous Rh2(OAc)4 catalysed sulfur transfer to these alkenes is also possible using propylene sulfide as the sulfur source. These methods did not give useful yields of products with alternative types of alkene substrate.A novel type of chiral lithium amide base reaction, involving the rearrangement of certain types of symmetrical ring-fused episulfoxides, gives alkenyl sulfoxide products in up to 88% ee. The structures of the products, including absolute stereochemistry, were assigned based on X-ray crystal structure determinations. p
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