What s sharpless asymmetric epoxidation?
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The Sharpless epoxidation response is an enantioselective substance response to plan 2,3-epoxyalcohols from essential and optional allylic alcohols . Enantioselectivity is accomplished by an impetus shaped from titanium tetra and diethyl tartrate .
The Sharpless epoxidation is suitable with a huge scope of essential and optional olefinic alcohols. Moreover, with the special case noted over, a given dialkyl tartrate will specially add to a similar face free of the substitution on the olefin .
The Sharpless epoxidation is suitable with a huge scope of essential and optional olefinic alcohols. Moreover, with the special case noted over, a given dialkyl tartrate will specially add to a similar face free of the substitution on the olefin .
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Sharpless Epoxidation reaction is an enantio-selective type reaction which is used to prepare 2,3-epoxy alcohols by reacting primary and secondary allyic alcohol.
This is also referred to as ring forming reaction.
It was named after Karl Barry Sharpless who received Noble Prize in chemistry in the year 2001.
This type of reaction is famous because of its success rate which depends on several factors.
Notable among the factors is that its reactants are easily available and are inexpensive.
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