1983
DOI: 10.1002/chin.198328169
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ChemInform Abstract: OPTICALLY ACTIVE C7‐SYNTHONS FOR LEUKOTRIENES A4

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“…Ϫ [α] D 20 ϭ Ϫ34.0 (c ϭ 1, CH 2 Cl 2 ) {ref. [30] [α] D 20 ϭ Ϫ32.7 (c ϭ 0.75, CHCl 3 )}. (2R,3R)-Epoxy-7-octen-1-ol (15a): Following the same procedure as described for the preparation of compound 15 but using dimethyl (Ϫ)-tartrate instead of dimethyl (ϩ)-tartrate, compound 13 was transformed to compound 15a.…”
Section: 7-octadien-1-ol (13)mentioning
confidence: 99%
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“…Ϫ [α] D 20 ϭ Ϫ34.0 (c ϭ 1, CH 2 Cl 2 ) {ref. [30] [α] D 20 ϭ Ϫ32.7 (c ϭ 0.75, CHCl 3 )}. (2R,3R)-Epoxy-7-octen-1-ol (15a): Following the same procedure as described for the preparation of compound 15 but using dimethyl (Ϫ)-tartrate instead of dimethyl (ϩ)-tartrate, compound 13 was transformed to compound 15a.…”
Section: 7-octadien-1-ol (13)mentioning
confidence: 99%
“…[29] Tolstikov et al described a different route from (E)-2,7-octadienol. [30] A stereospecific route to (E)-2,7-octadienol from the propargyl alcohol, involving a selective trans reduction with Li in liquid NH 3 , has also been reported. [31] …”
Section: Introductionmentioning
confidence: 99%