Alkylidenebutenolides from a 2-(Trimethylsiloxy)furan and Iodomethacrolein -Stereoselective Synthesis of Z-and E-Freelingyne. -Via an aldol/β-elimination approach as key sequence the title products such as (V) and (VI) are prepared. It is noteworthy that an earlier described method with triflic anh
✦ LIBER ✦
Z- or E-configurated γ-alkylidenebutenolides from a 2-(trimethylsiloxy)furan and iodomethacrolein - stereoselective synthesis of Z- and E-freelingyne
✍ Scribed by Frank von der Ohe; Reinhard Brückner
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 142 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The )'-(t~-hydroxylalkyl)butenolides lk-5 and ul-5 were prepared by Mukaiyama aldol additions between iodoaldehyde 10 and the trimethylsiloxy-substituted furan 6 in the presence of BF3eOEt2 and ZnBr2, respectively. Couplings of these butenolides with 3-ethynylfuran followed by anti-eliminations
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