PdCl 2 /NaI-Catalyzed Homodimeric Coupling-Cyclization Reaction of 2,3-Allenols: An Efficient Synthesis of 4-(1‘,3‘-Dien-2‘-yl)-2,5-dihydrofuran Derivatives
✍ Scribed by Deng, Youqian; Yu, Yihua; Ma, Shengming
- Book ID
- 120294989
- Publisher
- American Chemical Society
- Year
- 2008
- Tongue
- English
- Weight
- 110 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0022-3263
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## Abstract Transition‐metal‐catalyzed dimeric coupling–cyclization reactions of two different 2,3‐allenols afforded 4‐(1′,3′‐dien‐2′‐yl)‐2,5‐dihydrofuran derivatives **3**. 2‐Substituted 2,3‐allenols **1** cyclized to form the 2,5‐dihydrofuran ring, whereas the 2‐unsubstituted 2,3‐allenols **2** p
## 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 of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
4-(2%-Alkenyl)-2,5-dihydrofurans can be efficiently synthesized via the PdCl 2 -catalyzed coupling-cyclization of allylic halides with 2,3-allenols in DMA at rt in moderate to good yields. The regioselectivity is different from that of the Pd(0)-catalyzed coupling-cyclization of organic halides with
## Abstract For Abstract see ChemInform Abstract in Full Text.