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STUDIES ON THE STEREO-AND ENANTIOSELECTIVE SYNTHESIS OF 11.12-EPOXYSARCOPHYTOL-A,11,12-EPOXYSARCOPHYTOL-A ACETATE AND 11,12-EPOXYCEMBRENE-C.-SYNTHESIS OF 5,9,13-TRIMETHYL-2-ISOPROPYL-12(S),12(S)-EPOXY-14

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摘要 An efficient Synthesis of 5, 9, 13-trimethy1-2-isopropyl-12(S),13 (S)-epoxy-14-bromo-2 (Z), 4 (E). 8 (E)-tetradecatrienenitrile,a key intermediate in the synthesis of antitumor cembranoids including 11,12-epoxy-sarcophytol-A,11,12-epoxysarcophytol-A acetate and 11,12-epoxycembrene-C,was first describedthrough seven step sequence in-32% overall yield from E,E-farnesol. An efficient Synthesis of 5, 9, 13-trimethy1-2-isopropyl-12(S),13 (S)-epoxy-14-bromo-2 (Z), 4 (E). 8 (E)-tetradecatrienenitrile,a key intermediate in the synthesis of antitumor cembranoids including 11,12-epoxy-sarcophytol-A,11,12-epoxysarcophytol-A acetate and 11,12-epoxycembrene-C,was first describedthrough seven step sequence in-32% overall yield from E,E-farnesol.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 1995年第3期189-192,共4页 中国化学快报(英文版)
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