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ChemInform Abstract: Gold(I)‐Catalyzed Furan‐yne Cyclizations Involving 1, 2‐Rearrangement: Efficient Synthesis of Functionalized 1‐Naphthols and Its Application to the Synthesis of Wailupemycin G. Issue 10 (March 2015)
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Journal Article
Title:
ChemInform Abstract: Gold(I)‐Catalyzed Furan‐yne Cyclizations Involving 1, 2‐Rearrangement: Efficient Synthesis of Functionalized 1‐Naphthols and Its Application to the Synthesis of Wailupemycin G. Issue 10 (March 2015)
Main Title:
ChemInform Abstract: Gold(I)‐Catalyzed Furan‐yne Cyclizations Involving 1, 2‐Rearrangement: Efficient Synthesis of Functionalized 1‐Naphthols and Its Application to the Synthesis of Wailupemycin G.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>A novel gold‐catalyzed reaction of furan‐ynes bearing a propargylic alcohol moiety leads to multisubstituted 1‐naphthols via a cyclization/1, 2‐rearrangement cascade.</p> </abstract>