Enantioselective Total Synthesis of Bistramide A

Michael T. Crimmins, Amy C. DeBaillie

Journal of the American Chemical Society · 2006 · 96 citations · 26 references

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Abstract

The enantioselective synthesis of bistramide A has been achieved with a longest linear sequence of 18 steps. The synthetic strategy involves the use of a distereoselective glycolate alkylation, an aldol addition of a chlorotitanium enolate of N-acylthiazolidinthione, and a Sharpless asymmetric epoxidation to synthesize the three key fragments.

References

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