Synthesis of Diaryl Diselenides Having Chiral Pyrrolidine Rings with C2 Symmetry. Their Application to the Asymmetric Methoxyselenylation of trans-β-Methylstyrenes

DOI: 10.1246/cl.1994.923

Source and publish data:

Chemistry Letters p. 923 - 926 (1994)

Update date:2022-08-02

Topics:

Authors:

Fujita, Ken-ichi

Iwaoka, Michio

Tomoda, Shuji

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Article abstract of DOI:10.1246/cl.1994.923

Optically active diaryl diselenides carrying C₂ symmetrical chiral pyrrolidines are synthesized by the condensation between 2,2'-diselenobis(benzyl chloride) derivatives and chiral pyrrolidines and are applied to methoxyselenylation of trans-ol

Full text of DOI:10.1246/cl.1994.923

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Product name:N,N'-(diselenodi-2,1-phenylenemethylene)bis<(2R,5R)-bis(benzyloxymethyl)pyrrolidine>

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