Reaction of Tin Enolates with Substituted Tricarbonylcyclohexadienyliumiron Hexafluorophosphate Electrophiles: Diastereoselective Synthesis of (+/-)-Trichodiene

DOI: 10.1039/c39870001445

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1445 - 1447 (1987)

Update date:2022-07-29

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Authors:

Pearson, Anthony J.

O'Brien, Michael K.

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Article abstract of DOI:10.1039/c39870001445

A number of tin enolates react cleanly with tricarbonylcyclohexadienyliumiron cations, in cases where the use of lithium enolates or silyl enol ethers is problematic; this new carbon-carbon bond-forming reaction allows diastereoselective construction of p

Full text of DOI:10.1039/c39870001445

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