These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Highly active organocatalysts for asymmetric anti-Mannich reactions.
    Author: Martín-Rapún R, Fan X, Sayalero S, Bahramnejad M, Cuevas F, Pericàs MA.
    Journal: Chemistry; 2011 Aug 01; 17(32):8780-3. PubMed ID: 21735502.
    Abstract:
    Lighten the load! A family of enantiopure 4-oxy-substituted 3-aminopyrrolidines arising from the enantioselective ring-opening of meso-3-pyrroline oxide have been developed as catalysts for the asymmetric, anti-selective Mannich reaction (see scheme; PMP=p-methoxyphenyl; PG=protecting group). Very high catalytic activity (down to 0.01 mol % loading) and stereoselectivity have been recorded.
    [Abstract] [Full Text] [Related] [New Search]