Literature DB >> 10649344

Enantioselective

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Abstract

Even with only a catalytic amount of chiral bis(dihydrooxazole) 1 as external ligand, the rearrangement of benzyl ethers to alcohols [Eq. (1)] proceeds with high enantioselectivity (over 60 % ee). This reaction represents the first example of an enantioselective [1,2] Wittig rearrangement.

Entities:  

Year:  1999        PMID: 10649344     DOI: 10.1002/(sici)1521-3773(19991216)38:24<3741::aid-anie3741>3.0.co;2-5

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Further Studies on the [1,2]-Wittig Rearrangement of 2-(2-Benzyloxy)aryloxazolines.

Authors:  R Alan Aitken; Andrew D Harper; Ryan A Inwood
Journal:  Molecules       Date:  2022-05-17       Impact factor: 4.927

2.  Access to Diarylmethanols by Wittig Rearrangement of ortho-, meta-, and para-Benzyloxy-N-Butylbenzamides.

Authors:  R Alan Aitken; Andrew D Harper; Ryan A Inwood; Alexandra M Z Slawin
Journal:  J Org Chem       Date:  2022-03-14       Impact factor: 4.354

  2 in total

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