16863-62-0Relevant articles and documents
An enantioselective synthesis of (R)-5,6-octadecadienoic acid
Yu, Qiong,Ma, Shengming
, p. 1596 - 1601 (2015)
A convenient, scalable, and highly enantioselective total synthesis of (R)-5,6-octadecadienoic acid was developed by using the recently established ATA (allenylation of terminal alkynes) reaction of TBS-protected (TBS = tert-butyldimethylsilyl) propargyl alcohol with n-dodecanal in the presence of (R)-α,α-diphenylprolinol as the chiral source. The axial chirality of the allene unit withstood the many common organic transformations that were needed to achieve the total synthesis with a high ee (enantiomeric excess) value.
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Landor,S.R.,Punja,N.
, p. 4905 - 4907 (1966)
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