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... 4882. ) the reagent 22 for Mitsunobu coupling. The stereochemical course of this ... with simple acyclic secondary alcohols such as 21 was not reported. Salvatore D. ...
URL: https://www.organic-chemistry.org/Highlights/2009/21September.shtm
... a Wittig olefination , and lastly a Mitsunobu macrolactonisation previously used by Tony Barrett in ... Organic Chemistry Portal Reactions >> Total Syntheses Totally Synthetic by Paul H. ...
URL: https://www.organic-chemistry.org/totalsynthesis/totsyn01/milbemycin-o-doherty.shtm
... alcohol 8, that was coupled under Mitsunobu conditions with the phenol 9 to give ... a Grob fragmentation, in fact this reaction was developed (J . Org. ...
URL: https://www.organic-chemistry.org/Highlights/2014/07April.shtm
... the hydroxyl was done with a typical Mitsunobu , with only a few more steps ... Organic Chemistry Portal Reactions >> Total Syntheses Totally Synthetic by Paul H. ...
URL: https://www.organic-chemistry.org/totalsynthesis/totsyn05/agelastatin-a-tanaka-yoshimitsu.shtm
... 9 to the monomethyl aniline 10. Mitsunobu esterification usually proceeds with inversion of absolute ... the terminal bromide 6 is a textbook reaction, it is little used. Hiroshi ...
URL: https://www.organic-chemistry.org/Highlights/2018/12March.shtm
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