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Merck
  • Desymmetrization of meso-dienyne by asymmetric Pauson-Khand type reaction catalysts.

Desymmetrization of meso-dienyne by asymmetric Pauson-Khand type reaction catalysts.

Chemical communications (Cambridge, England) (2004-04-30)
Nakcheol Jeong, Dong Hoon Kim, Jun Hun Choi
摘要

Desymmetrization of the meso dienynes, such as propargyl 1-vinylallyl N-tosylamides (1a-c) and propargyl 1-vinylallyl ethers (1d-e), by asymmetric Pauson-Khand type reaction catalysts was studied. The corresponding vinyl substituted bicyclic pentenones (2 and 3) were obtained with high diastereoselectivity and enantioselectivity.

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Sigma-Aldrich
(R)-(+)-2,2′-双(二苯基膦)-1,1′-联萘, 97%
Sigma-Aldrich
1,4-戊二烯-3-醇, contains 0.4% hydroquinone as stabilizer, ≥96%