Stereoselective Synthesis of d-5-Homo-4-selenoribose as a Versatile Intermediate for 4鈥?Selenonucleosides
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文摘
Stereoselective synthesis of d-5-homo-4-selenoribose, serving as a versatile intermediate for the synthesis of 4鈥?selenonucleosides 12a鈥?b>c, was accomplished using Sharpless asymmetric epoxidation, regioselective cleavage of the 伪,尾-epoxide, and stereoselective reduction of the ketone as the key steps.

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