Stereoselective syntheses of "multifidenes" and related structures. 
Contribution to the synthetic chemistry of cis-disubstituted 
alken-1-ylcyclopentenes

Boland, W.; Jaenicke, L.

doi:10.1021/jo00394a016

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Stereoselective syntheses of "multifidenes" and related structures. Contribution to the synthetic chemistry of cis-disubstituted alken-1-ylcyclopentenes

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Boland, W., & Jaenicke, L. (1979). Stereoselective syntheses of "multifidenes" and related structures. Contribution to the synthetic chemistry of cis-disubstituted alken-1-ylcyclopentenes. Journal of Organic Chemistry, 44(26), 4819-4824. doi:10.1021/jo00394a016.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0012-9F07-A

Abstract

Multifidene 8b, a major constituent of the essential oil of the seaweed, Cutleria multifida, was recognized as a chemical signal for gamete union. To test the specificity of the plant receptor system, a new synthesis for structures like 8b was developed