1999
DOI: 10.1002/chin.199913081
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ChemInform Abstract: Regio‐ and Diastereoselective Allenylation of Aldehydes in Aqueous Media: Total Synthesis of (+)‐Goniofufurone.

Abstract: ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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 via the “References” option.

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“…In contrast, when propargyl bromide was γ-substituted the coupling products were predominantly, or exclusively, the allenylic alcohols. Li et al examined the propargylation-allenylation of carbonyl compounds using a variety of metals including Sn, Zn, Bi, Cd and In [29]. By using the indium-mediated allenylation reaction, Li and co-workers developed the synthesis of the anti-viral, anti-tumor compound (+)-goniofufurone [30] (eq.…”
Section: Introductionmentioning
confidence: 98%
“…In contrast, when propargyl bromide was γ-substituted the coupling products were predominantly, or exclusively, the allenylic alcohols. Li et al examined the propargylation-allenylation of carbonyl compounds using a variety of metals including Sn, Zn, Bi, Cd and In [29]. By using the indium-mediated allenylation reaction, Li and co-workers developed the synthesis of the anti-viral, anti-tumor compound (+)-goniofufurone [30] (eq.…”
Section: Introductionmentioning
confidence: 98%