From tartrate to taxoids: A double, intramolecular Diels-Alder strategy
نویسندگان
چکیده
منابع مشابه
The first intramolecular silene Diels-Alder reactions.
The synthesis of silaheterocycles through the first examples of an intramolecular silene Diels-Alder reaction is described.
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Trienes 1 and 3 were obtained in five steps from ethyl 4-acetoxy-3-oxobutanoate and 6-iodo-3-methyl-1,3-hexadiene. Intramolecular Diels-Alder cyclization of 1 and 3 gave tricyclic lactones 2 and 4 as the major products, respectively. The key intermediate 4 was converted in two steps to trans-dihydroconfertifolin (5).
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چکیده: هدف اصلی این مطالعه ی توصیفی تحقیقی در حقیقت تلاشی پساروش-گرا به منظور رسیدن به نتیجه ای منطقی در انتخاب مناسبترین راهکار آموزشی بر گرفته از چارچوب راهبردی مطرح شده توسط والدمر مارتن بوده که به بهترین شکل سازگار و مناسب با سامانه ی آموزشی ایران باشد. از این رو، دو راهکار آموزشی، راهکار ارتباطی و راهکار بازساختی، برای تحقیق و بررسی انتخاب شدند. صریحاً اینکه، در راستای هدف اصلی این پژوهش، ر...
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A fascinating aspect of the Diels–Alder reaction is its endo selectivity. This endo preference is much less pronounced in intermolecular cases compared with the intramolecular and transannular Diels–Alder (IMDA and TADA) reactions. Nevertheless, high endo selectivity is observed in the Diels– Alder additions of (E)-1-O-substituted dienes catalyzed by Lewis acids that lead to cis-1,6-disubstitut...
متن کاملDiels-Alder cycloaddition strategy for kinetic resolution of chiral pyrazolidinones.
A rare example of the application of a catalytic, enantioselective Diels-Alder cycloaddition to affect a kinetic resolution has been developed. Chiral pyrazolidinones are resolved with high selectivity through a process that utilizes a relay of stereochemical information from a permanent chiral center to a fluxional chiral center to enhance the inherent selectivity of the chiral Lewis acid cata...
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ژورنال
عنوان ژورنال: Pure and Applied Chemistry
سال: 1997
ISSN: 1365-3075,0033-4545
DOI: 10.1351/pac199769030495