2004
DOI: 10.1007/s11172-005-0076-z
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Synthesis of dendrimers with terminal formyl groups

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Cited by 25 publications
(11 citation statements)
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References 19 publications
(17 reference statements)
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“…CESL was separated using the same method, where five alkaloids ( 1 – 5 ) and two phenolic compounds ( 6 and 7 ) were isolated. The isolated compounds were identified as N , N ‐dimethylanthranilic acid ( 1 ), N ‐(4‐hydroxyphenyl)acetamide ( 2 ), 2‐(methylamino)benzoic acid ( 3 ), nicotinamide ( 4 ), 2,3‐dihydro‐4,6‐dihydroxy‐1 H ‐isoindol‐1‐one ( 5 ), 5,7‐dihydroxyisobenzofuran‐1(3 H )‐one ( 6 ), 5‐(hydroxymethyl)‐1,3‐benzenediol ( 7 ), and (7 Z ,10 Z )‐7,10‐octadecadienoic acid methyl ester ( 8 ) by comparison of spectroscopic and LC/MS data with the reported values ( Figure ). To the best of our knowledge, this study reports the identification of compound 8 for the first time from C .…”
Section: Resultsmentioning
confidence: 99%
“…CESL was separated using the same method, where five alkaloids ( 1 – 5 ) and two phenolic compounds ( 6 and 7 ) were isolated. The isolated compounds were identified as N , N ‐dimethylanthranilic acid ( 1 ), N ‐(4‐hydroxyphenyl)acetamide ( 2 ), 2‐(methylamino)benzoic acid ( 3 ), nicotinamide ( 4 ), 2,3‐dihydro‐4,6‐dihydroxy‐1 H ‐isoindol‐1‐one ( 5 ), 5,7‐dihydroxyisobenzofuran‐1(3 H )‐one ( 6 ), 5‐(hydroxymethyl)‐1,3‐benzenediol ( 7 ), and (7 Z ,10 Z )‐7,10‐octadecadienoic acid methyl ester ( 8 ) by comparison of spectroscopic and LC/MS data with the reported values ( Figure ). To the best of our knowledge, this study reports the identification of compound 8 for the first time from C .…”
Section: Resultsmentioning
confidence: 99%
“…Many publications and patents have reported preparations of magnetic and conductive polymers and functionalized copolymers [37][38][39][40][41][42][43][44][45][46][47][48][49], dendrimers [50,51], dyes [52,53] and chemiluminiscent materials too [54]. Other interesting data such as molecular polarizability, energies, electrochemical properties, half-time of fluorescence or phosphorescence, etc., have been reported too .…”
Section: History and Synthesis Of Pentafluorobenzaldehydementioning
confidence: 99%
“…J-coupling constant of the anomeric C-H. Aryl glycosylation gave aldehyde 20c, which was condensed with ʟ-cysteine methyl ester hydrochloride, acylated and cyclised to afford tetramate 21.Due to the acid-labile nature of phenyl glycosides prepared above and the resulting difficulty associated with the acidic work-up procedure required to remove chelating metal ions, an alternative route to the incorporation of glycones via a benzyl alcohol linking group was explored (Scheme 8).The controlled reduction of terephthalaldehyde with NaBH 4 between 0-2°C afforded 4-(hydroxymethyl)benzaldehyde in 70 % yield according to a modified literature procedure 52. Lewis acid-catalysed glycosylation with β-D-galactosepentaacetate 15a gave aldehyde 22 as the β-anomer in 71% yield along with the byproduct 4-(acetoxymethyl)benzaldehyde in 28 % yield.…”
mentioning
confidence: 99%