Chiral Chalcogen Peptides as Ligands for the Catalytic Enantioselective Aryl Transfer Reaction to Aldehydes
A new series of chiral chalcogen peptides were synthesized from inexpensive and commercially available starting materials. The synthesized compounds were tested as catalysts in the enantioselective arylation of aldehydes by using arylboronic acids as the aryl source. The desired diarylmethanols were...
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Veröffentlicht in: | European Journal of Organic Chemistry 2010-07, Vol.2010 (19), p.3574-3578 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A new series of chiral chalcogen peptides were synthesized from inexpensive and commercially available starting materials. The synthesized compounds were tested as catalysts in the enantioselective arylation of aldehydes by using arylboronic acids as the aryl source. The desired diarylmethanols were obtained in excellent yields and with enantioselectivities up to 91 % ee.
A new class of chiral chalcogen peptide based ligands was prepared and applied in the zinc‐catalyzed addition of arylboronic acids to aldehydes. The chiral diarylmethanol products were obtained in excellent yields and with a high level of enantioselectivity up to 91 % ee. |
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ISSN: | 1434-193X 1099-0690 |
DOI: | 10.1002/ejoc.201000237 |