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ChemInform Abstract: Facile Formation of Tetrahydrofurans with Multiple Chiral Centers Using Double Iodoetherification of σ-Symmetric Diene Acetals: Short Asymmetric Total Synthesis of Rubrenolide (VIII) and Rubrynolide (IX).

✍ Scribed by Hiromichi Fujioka; Yusuke Ohba; Hideki Hirose; Kenji Nakahara; Kenichi Murai; Yasuyuki Kita


Publisher
John Wiley and Sons
Year
2008
Weight
46 KB
Volume
39
Category
Article
ISSN
0931-7597

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A Double Iodoetherification of σ-Symmetr
✍ Hiromichi Fujioka; Yusuke Ohba; Hideki Hirose; Kenichi Murai; Yasuyuki Kita 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 127 KB 👁 1 views

Many biologically active natural products contain multiple chiral centers and occur in their optically active form, and therefore the development of methodologies that can lead to multiple chiral centers is desirable in synthetic organic chemistry. Recently, we developed the intramolecular haloether