2000
DOI: 10.1021/jo991624u
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Masked Formylation with 2-Benzotriazolyl-1,3-dioxolane, a Novel Formyl Cation Equivalent

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Cited by 23 publications
(9 citation statements)
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“…1-(Chloromethyl)benzotriazole reacted with sodium dialkyl phosphites to give dialkyl-(1-benzotriazolmethyl)phosphonates 123, which are potential Horner-Emmons reagents [178] for the stereoselective preparation of (E)-1-(1-alkenyl)benzotriazoles [179]. 2-Benzotriazolyl-1,3-dioxolane (124) has been utilized as a novel formyl cation equivalent [180]. The novel three-carbon synthon 1-(1H-1,2,3-benzotriazol-1-yl)-3-chloroacetone (125) (112), and alkylthio- (113) methylbenzotriazoles [167].…”
Section: Benzotriazole-mediated Imidoylationmentioning
confidence: 99%
“…1-(Chloromethyl)benzotriazole reacted with sodium dialkyl phosphites to give dialkyl-(1-benzotriazolmethyl)phosphonates 123, which are potential Horner-Emmons reagents [178] for the stereoselective preparation of (E)-1-(1-alkenyl)benzotriazoles [179]. 2-Benzotriazolyl-1,3-dioxolane (124) has been utilized as a novel formyl cation equivalent [180]. The novel three-carbon synthon 1-(1H-1,2,3-benzotriazol-1-yl)-3-chloroacetone (125) (112), and alkylthio- (113) methylbenzotriazoles [167].…”
Section: Benzotriazole-mediated Imidoylationmentioning
confidence: 99%
“…The major isomer was purified by chromatography on silica gel. Cyanobenzyl)-1,3-dioxolane (7d): [42] Isomer 7d was obtained in 92 % (0.174 g) isolated yield. Nitrobenzyl)-1,3-dioxolane (8d): [43] Isomer 8d was obtained in 87 % (0.182 g) isolated yield.…”
Section: General Procedures For the Coupling Of Enol Ethers With Aryl mentioning
confidence: 99%
“…[44] Isomer 9d was obtained in 90 % (0.209 g) isolated yield. 1 [42] and Products 11b, 11c and 11e: A mixture of isomers 11b-e was obtained in 87 % (0.191 g) isolated yield. …”
Section: General Procedures For the Coupling Of Enol Ethers With Aryl mentioning
confidence: 99%
“…Moreover, during the multistep synthesis of many natural products, formylation reaction is often necessary, and the selectivity, simplicity, and efficiency of this step are highly critical . Some of the widely used formylating agents that have been reported up to now are POCl 3 / N , N ‐dimethylformamide (DMF) , HCO 2 H/ N,N′ ‐Dicyclohexylcarbodiimide (DCC) , 2,2,2‐trifluoroethyl formate , formic acid/1‐Ethyl‐3‐(3‐dimethylaminopropyl)carbodiimide (EDAC) , acetic formic anhydride , formyl‐pivaloyl anhydride , cyanomethylformate , pentafluorophenyl formate , imidazole/DMF , MeOH/Ru , CO 2 /PhMe 2 SiH , AgOTf/Cl 2 CHOMe , tetramethylethylenediamine/O 2 /visible light , FeCl 3 /DMSO , CO/acid , 2‐benzotriazolyl‐1,3‐dioxolane , N ‐methyl aniline/Ru , Pd/CO/H 2 , tert ‐butyl isocyanide , Pd/CH 3 NO 2 , etc. In spite of the diversity of formylating agents, there are serious restrictions for the preparation of some of them, such as harsh experimental conditions, the use of unusual reagents, formation of unwanted or toxic byproducts, use of expensive procedures for their synthesis, and thermal instability of the reagents.…”
Section: Introductionmentioning
confidence: 99%