Literature DB >> 15045076

Aminative rearrangement of 2-alkoxy-3,4-dihydro-2H-pyrans: a novel stereocontrolled route to substituted pyrrolidines.

Alan Armstrong1, Graham R Cumming, Kurt Pike.   

Abstract

Aziridination of 2-alkoxy-3,4-dihydro-2H-pyrans leads to rearrangement and stereocontrolled formation of 5-alkoxypyrrolidines which may be reduced to pyrrolidines or allylated stereoselectively.

Entities:  

Year:  2004        PMID: 15045076     DOI: 10.1039/b316554j

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  Trifluoromethanesulfonamide vs. Non-Fluorinated Sulfonamides in Oxidative Sulfamidation of the C=C Bond: An In Silico Study.

Authors:  Anton V Kuzmin; Mikhail Yu Moskalik; Bagrat A Shainyan
Journal:  Molecules       Date:  2020-10-22       Impact factor: 4.411

  1 in total

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