A novel D + BCD + ABCD route to ll-keto steroids is reported involving a high yield stereoselective intramolecular Diels-Alder reaction of furan-diene 5a in water as a key-step. The dienophilic side chain is readily introduced starting from 2 via a sequence involving alkylation with ethyl 4-iodo-3-
✦ LIBER ✦
Synthesis, Characterization, and Intramolecular Diels—Alder Reaction Tandem Dehydroaromatization of a Diene-diyne.
✍ Scribed by Shu-Zhi Liu; Guang-Shi Tang; Jing Wang; Xue-Hua Li
- Book ID
- 101983684
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 15 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
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## Abstract For Abstract see ChemInform Abstract in Full Text.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.