Abstract
The gold-catalysed coupling of allyl sulfides with propargylic
carboxylates follows different pathways depending upon the choice
of nonmigrating group on the sulfur and the aromatic group at the
propargylic position of the alkyne substrate.
Key words
gold - sulfur ylides - alkynes - propargylic
carboxylates - coupling
References and Notes
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Only very limited success has been
observed with aliphatic substituents at the propargylic position.
Aldehyde-derived systems are observed to give only trace amounts
of con- version or undergo degradation. Ketone derivative A-1 proceeds sluggishly to give the desired
coupling product
A-3a in low
yield (Scheme
[6 ]
).
Scheme 6
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Similarly, neither (E )-
or (Z )-6gd were
observed when 3gd was added to an ongoing
reaction.