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|Title:||Stereocontrolled synthesis of linear 22R-homoallylic sterols via a triflic acid-catalyzed 2-oxonia cope rearrangement||Authors:||Loh, T.-P.
|Issue Date:||11-Jul-2002||Citation:||Loh, T.-P., Hu, Q.-Y., Ma, L.-T. (2002-07-11). Stereocontrolled synthesis of linear 22R-homoallylic sterols via a triflic acid-catalyzed 2-oxonia cope rearrangement. Organic Letters 4 (14) : 2389-2391. ScholarBank@NUS Repository. https://doi.org/10.1021/ol026136e||Abstract:||(Matrix presented) Poor stereoselectivity caused by the involvement of side reaction pathways was observed in the In(OTf)3-catalyzed allyl-transfer reaction (R = electron-withdrawing group). Subsequently, it was found that the employment of triflic acid (TFA) as catalyst could successfully suppress the side reaction pathways and, hence, achieve high stereoselectivity.||Source Title:||Organic Letters||URI:||http://scholarbank.nus.edu.sg/handle/10635/94878||ISSN:||15237060||DOI:||10.1021/ol026136e|
|Appears in Collections:||Staff Publications|
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