期刊
ORGANIC LETTERS
卷 10, 期 22, 页码 5313-5316出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol802266s
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-
资金
- National Institutes of Health [GM026782]
The synthesis and intramolecular Diels-Alder reactions of trienes 5 and 6 with a siloxacyclopentene-constrained dienophile are described. These reactions provide the primary cycloadducts 7 and 8 with high diastereoselectivity. These cycloadducts possess trans-relationships between the ring fusion proton and the adjacent C(1) alkoxy group and can be further elaborated to alcohols 9 and 11 (via protiodesilylation) or to 10 and 12 (via Fleming-Tamao oxidation) depending on the substitutent R.
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