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|Title:||Short synthetic route to retinoids through dialkylation of 3-methyl-3-sulfolene|
|Publisher:||PERGAMON-ELSEVIER SCIENCE LTD|
|Citation:||TETRAHEDRON LETTERS, 38(14), 2585-2586|
|Abstract:||The C-20-retinoid carbon skeleton has been synthesised through sequential alkylations of 3-methyl-3-sulfolene with bromomethyl methyl ether followed by C-14-aldehyde to give dialkyl sulfolene which on further desulfonylation and dehydration yielded retinol methyl ether. (C) 1997 .|
|Appears in Collections:||Article|
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