Allylic polyprenols synthesis

Solanesol and other prenyl alcohols are important as metabolites in mulberry and tobacco leaves and in the synthesis of isoprenoid quinones. Hence, Sato and collaborators107 have developed a stereoselective synthesis of all-trans-polyprenol alcohols up to C50. Construction of the requisite skeletons was accomplished by the alkylation of a p-toluenesulphonyl-stabilized carbanion, followed by reductive desulphonylation of the resulting allylic sulphonyl group. This was achieved most efficiently by the use of a large excess of lithium metal in ethylamine (equation (43)), although all reaction conditions led to mixtures. The minor product results from double bond rearrangement. 

Asymmetric hydrogenation of allylic alcohols (14, 39-40).1 Mammalian dol-ichols (2) are terminal dihydropolyisoprenols which are involved in glycoprotein synthesis. They contain one terminal chiral primary allylic alcohol group. The polyprenols 3 present in plants correspond to dolichols except that they lack the terminal double bond considered to be (Z). They can be obtained by hydrogenation of 2 catalyzed by (bistrifluoroacetate)ruthenium(II) and (S)-l, which affects only the terminal double bond to provide (S)-3 in >95% ee. 

The role of undecaprenyl phosphate (C55, allylic) as a carrier of glycosyl units in the biosynthesis of bacterial cells walls is well established. Dolichyl phosphate plays a similar role in the synthesis of glycoproteins in animal systems. Evidence that prenyl lipids serve as glycosyl carriers in the biosynthesis of glycoproteins in plants is accumulating rapidly (Pont Lezica et al., 1976 Delmer al., 1978 Erickson et al., 1978). Several authors have recently reviewed the literature on the role of polyprenols as glycosyl carriers in plants (Hemming, 1978 Pont Lezica, 1979 Elbein, 1979). 

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