Methylene-bis-tartronates and methylene-bis-hydroxymethylmalonates form monolactones where the CO(2)R and OH (or CH2OH) groups are known to be cis-oriented. However, attempts to prepare the corresponding dilactones failed due to the unsufficient proximity of these functional groups. The results have been confirmed by NMR spectra.
Methylene-bis-tartronates and methylene-bis-hydroxymethylmalonates form monolactones where the CO(2)R and OH (or CH2OH) groups are known to be cis-oriented. However, attempts to prepare the corresponding dilactones failed due to the unsufficient proximity of these functional groups. The results have been confirmed by NMR spectra.
作者:R. G. Kostyanovsky、Yu. I. El'natanov、O. N. Krutius
DOI:10.1007/bf00700172
日期:1994.12
Treatment of alkylenebismalonates with NaH and benzoyl peroxide afforded dibenzoyloxy derivatives. Alkaline hydrolysis of the latter gave alkylenebistartronic acids. Tetramethyl and tetraethyl esters and tetraamides of these acids were synthesized.
Kostjanowskiii R. G., Elnatanow Ju. I., Krutius O. N., Isw. AN. Ser. khim., (1994) N 12, S 2190-2193
作者:Kostjanowskiii R. G., Elnatanow Ju. I., Krutius O. N.
DOI:——
日期:——
Autoassembly of cage structures
作者:R. G. Kostyanovsky、Yu. I. El'natanov、O. N. Krutius、I. I. Chervin
DOI:10.1007/bf00696323
日期:1994.11
Methylene-bis-tartronates and methylene-bis-hydroxymethylmalonates form monolactones where the CO(2)R and OH (or CH2OH) groups are known to be cis-oriented. However, attempts to prepare the corresponding dilactones failed due to the unsufficient proximity of these functional groups. The results have been confirmed by NMR spectra.