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

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

DOI Full Paper Access

10

Citations

13

References

1997

Year

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

Tetrahedron Letters

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

	Year	Citations

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