Highly stereoselective epoxidation of a 4-methyl-5- (triethylsilyl)oxyallyl alcohol system with m-chloroperoxybenzoic acid

DOI: 10.1016/S0040-4039(98)00804-1

Source and publish data:

Tetrahedron Letters p. 4517 - 4520 (1998)

Update date:2022-09-26

Topics:

Authors:

Maruyama, Kimiyuki

Ueda, Masato

Sasaki, Shinobu

Iwata, Yasuhiro

Miyazawa, Masahiro

Miyashita, Masaaki

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Article abstract of DOI:10.1016/S0040-4039(98)00804-1

Epoxidation of 4-methyl-5-(triethylsilyl)oxyallyl alcohol system with m- chloroperoxybenzoic acid (MCPBA) has been found to occur highly stereoselectively and in high yields from the opposite side of the C₅ triethylsilyloxy group regardless of

Full text of DOI:10.1016/S0040-4039(98)00804-1

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