10536-76-2Relevant articles and documents
Durst
, p. 2421 (1974)
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Neish,Lemieux
, p. 454,457 (1952)
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A sustainable byproduct catalyzed domino strategy: Facile synthesis of α-formyloxy and acetoxy ketones via iodination/nucleophilic substitution/hydrolyzation/oxidation sequences
Zhu, Yan-Ping,Gao, Qing-He,Lian, Mi,Yuan, Jing-Jing,Liu, Mei-Cai,Zhao, Qin,Yang, Yan,Wu, An-Xin
supporting information; experimental part, p. 12700 - 12702 (2012/01/03)
The sustainable byproduct catalyzed domino strategy has been performed for the facile synthesis of α-formyloxy and acetoxy ketones via iodination/nucleophilic substitution/hydrolyzation/oxidation sequences from simple and readily available aromatic ketone
TRIS(3,6-DIOXAHEPTYL)AMINE AS A PHASE-TRANSFER CATALYST IN PHENACYL ESTER SYNTHESIS
Bartsch, Richard A.,Phillips, John B.
, p. 1777 - 1780 (2007/10/02)
Tris(3,6-dioxaheptyl)amine (TDA-1) may be substituted for toxic crown ethers in the phase-transfer catalyzed synthesis of phenacyl esters from weakly nucleophilic potassium carboxylates and α,p-dibromoacetophenone in acetonitrile.