Selective epoxidation of monoterpenes with methyltrioxorhenium and H 2 O 2

ALP de Villa, DE De Vos, CC de Montes, PA Jacobs

文献索引：Villa De P., Aida L.; De Vos, Dirk E.; Montes De C., Consuelo; Jacobs, Pierre A. Tetrahedron Letters, 1998 , vol. 39, # 46 p. 8521 - 8524

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被引用次数: 13

摘要

In the presence of pyridine as a co-catalyst, CH3ReO3 catalyses the epoxidation of terpenes such as α-pinene with H2O2 with minimal rearrangement of the epoxide. Pyridine is also critical to suppress isomerisation of the olefin substrate (in case of nerol, geraniol). The reaction can be directed towards selective single or double epoxidation, or in one step towards the rearranged product (eg from linalool to the ring-closure product linalool oxide).