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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


📜 SIMILAR VOLUMES


ChemInform Abstract: Z- or E-Configurate
✍ F. VON DER OHE; R. BRUECKNER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

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