Concepedia

An approach to chiral tri-substituted olefins: Synthesis of the C(1)C(7) segment of halichomycin

Erin E. McCann, Glenn Janes, Craig Ortsey, John L. Wood

Tetrahedron Letters · 1997 · 10 citations · 13 references

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Concepts

Abstract

A two step, stereocontrolled procedure has been developed for production of 2, a precursor to the C(1)C(7) segment of halichomycin (1).

References

13

Stereoselective aldol condensations via boron enolates

David A. Evans, J. V. Nelson, E. Vogel et al. · Journal of the American Chemical Society · 1981 · 509 citations

, , +7

Acyclic stereoselection. 48. Reversal of stereochemistry in the aldol reactions of a chiral boron enolate

Hidenori Danda, Marvin M. Hansen, Clayton H. Heathcock · The Journal of Organic Chemistry · 1990 · 149 citations

, , +7

Total synthesis of (-)-N-methylmaysenine

E. J. Corey, Leland O. Weigel, A. Richard Chamberlin et al. · Journal of the American Chemical Society · 1980 · 99 citations

, , +7

Cooperative effect by a hydroxy and ether oxygen in epoxidation with a peracid

Mark R. Johnson, Yoshito Kishi · Tetrahedron Letters · 1979 · 93 citations

, , +4

Total ssynthesis of (±) thiolactomycin

Chia‐Lin J. Wang, Joseph M. Salvino · Tetrahedron Letters · 1984 · 65 citations

, , +2