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Search results for: mitsunobu reaction

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... "green" equivalent to the chemical-intensive Mitsunobu inversion. see article for more examples ... mmol) - see article for more reactions proposed reaction pathway for (S ) ...
URL: https://www.organic-chemistry.org/abstracts/lit2/293.shtm
... upon oxidation can then be converted by Mitsunobu reaction to the target bicyclic structures, ... indolizidine 207A. Jeremy A. May at the University of Houston has shown ( ...
URL: https://www.organic-chemistry.org/Highlights/2012/26November.shtm
... Boc-protected sulfamides, followed by N-alkylation via Mitsunobu reaction to introduce more diversity. Silica-bonded ... acid (Si-TsOH) was used for Boc-removal, which was possible in 5 minutes ...
URL: https://www.organic-chemistry.org/Highlights/2005/15December.shtm
... /jo8000782) 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
... dimorpholide 18 as a reagent for the Mitsunobu coupling of 19 with 20. The ... an amine with the activated intermediate from reaction of an acid 16 with Xtal-Fluor E ...
URL: https://www.organic-chemistry.org/Highlights/2014/26May.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
... 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
... 8 delivered the allylic alcohol 9. Mitsunobu coupling of 9 with the phenol 5 ... alkenyl bromide 5. Although the Wittig reaction initially delivered 5 as a mixture of ...
URL: https://www.organic-chemistry.org/Highlights/2024/01April.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
... 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
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