Eremanthine衍生物α-亚甲基-γ-内酯的催化加氢和甲醇加成研究

J. Alves
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引用次数: 1

摘要

倍半萜内酯:愈创木-1(10)、11(13)-二烯-4α-羟基、9α-乙酰-15-碘-12、6α-内酯(2)、愈创木-1(10)、4(15)、11(13)-三烯-9α-羟基-12、6α-内酯(3)、(11S)-愈创木-4(15)、10(14)-二烯-9α-羟基-13-甲氧基-12、6α-内酯(4)、(11S)-愈创木-1(10)-烯-4α、9α-二羟基-13-甲氧基-12、6α-内酯(5)、和愈创木-1(10),11(13)-二烯-4α,9α-二羟基-15-碘-12,6α-内酯(6),从天然产物eremanthine(1)开始(1)。本文报道了烯丙基衍生物2-5的催化加氢反应和碘醇6的α-亚甲基-γ-内酯的甲醇加成反应。
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Study of Catalytic Hydrogenation and Methanol Addition to α-Methylene-γ-Lactone of Eremanthine Derivatives
The sesquiterpene lactones guaia-1(10),11(13)-dieno-4α-hydroxy,9α-acetyl-15-iodine-12,6α-lactone (2), guaia-1(10),4(15),11(13)-trieno-9α-hydroxy-12,6α-lactone (3), (11S)-guaia-4(15),10(14)-dieno-9α-hydroxy-13-methoxy-12,6α-lactone (4), (11S)-guai-1(10)-eno-4α,9α-dihydroxy-13-methoxy-12,6α-lactone (5), and guaia-1(10),11(13)-dieno-4α,9α-dihydroxy-15-iodine-12,6α-lactone (6) were previously obtained starting from the natural product eremanthine (1). In this paper we report the catalytic hydrogenation reactions of allylic derivatives 2–5 and the methanol addition to α-methylene-γ-lactone of the iodohydrin 6.
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