77987-27-0Relevant articles and documents
THE γ-ALKYLATION OF ENONES USING SILYL DIENOL ETHERS: THE EFFECT OF CHANGING THE ELECTROPHILE AND OF CHANGING THE SILYL GROUP
Fleming, Ian,Lee, Thomas V.
, p. 705 - 708 (1981)
Phenylthiomethyl chloride (3) and the trimethylsilyl dienol ether (2) of crotonophenone react to give the lowest level of γ-attack of a range of carbon electrophiles and trimethylsilyl dienol ethers; the γ-selectivity for this reaction can be raised from