ملخص
Short and efficient syntheses of two diastereomeric cyclopentane segments present in most jatrophane diterpenes were achieved. Key steps are a stereoselective C-2 elongation, an RCM, and a hydroboration reaction. An orthogonal protecting group methodology makes these segments useful building blocks for diterpene synthesis.
اللغة الأصلية | English |
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الصفحات (من إلى) | 5326-5328 |
عدد الصفحات | 3 |
دورية | Organic Letters |
مستوى الصوت | 11 |
رقم الإصدار | 22 |
المعرِّفات الرقمية للأشياء | |
حالة النشر | Published - 2009 |
منشور خارجيًا | نعم |
ASJC Scopus subject areas
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