406701-01-7Relevant academic research and scientific papers
The stereoselective synthesis of oxetanes; exploration of a new, Mitsunobu-style procedure for the cyclisation of 1,3-diols
Christlieb,Davies,Eames,Hooley,Warren
, p. 2983 - 2996 (2007/10/03)
A solution of 2-methyl-3-[1-(phenylsulfanyl)cyclohexyl]propane-1,3-diol 1 in toluene treated with triphenyl-phosphine, Ziram 2 and DEAD, gave 3-methyl-2-[1-(phenylsulfanyl)cyclohexyl]oxetane 3 in 85% yield. A mechanistic study has been undertaken, optimal conditions have been found and the range of substrates for which the reaction is useful has been explored. We include the results of an X-ray study which shows that compound 33 (the oxidation product of diol 1) is a sulfone rather than a sulfoxide as previously reported.
The scope and limitation of the [1,4]-SPh shift in the synthesis of allylic alcohols
Aggarwal, Varinder K.,Eames, Jason,De Las Heras, Maria A.,McIntyre, Sara,Warren, Stuart
, p. 4456 - 4461 (2007/10/03)
Treatment of a series of 4-phenylsulfanyl-1,3-diols with toluene-p-sulfonyl chloride in pyridine gives stereospecifically substituted allylic alcohols in near quantitative yield via a [1,4]-SPh shift. We comment on the structural variation at both the mig
