Dimethyl 2,2′‐[carbonylbis(Azanediyl)](2s,2′s)‐bis[3‐(4‐hydroxyphenyl)propanoate]

Antonio Palumbo Piccionello; Nicola Della Ca’; Carla Carfagna; Katia F. Gioia; Bartolo Gabriele; Raffaella Mancuso

Dimethyl 2,2′‐[carbonylbis(Azanediyl)](2s,2′s)‐bis[3‐(4‐hydroxyphenyl)propanoate]

Antonio Palumbo Piccionello, Nicola Della Ca’, Carla Carfagna, Katia F. Gioia, Bartolo Gabriele, Raffaella Mancuso

Scienze e Tecnologie Biologiche Chimiche e Farmaceutiche

Risultato della ricerca: Article › peer review

1 Citazioni (Scopus)

Abstract

The thus‐far unknown ureic derivative dimethyl 2,2′‐[carbonylbis(azanediyl)](2S,2′S)‐ bis[3‐(4‐hydroxyphenyl)propanoate] has been efficiently synthesized by enantiospecific oxidative carbonylation of readily available L‐tyrosine methyl ester, using a very simple catalytic system (PdI2 in conjunction with KI) under relatively mild conditions (100 °C for 5 h in DME as the solvent and under 20 atm of a 4:1 mixture CO‐air).

Lingua originale	English
pagine (da-a)	M983-
Numero di pagine	3
Rivista	MolBank
Volume	2018
Stato di pubblicazione	Published - 2018

All Science Journal Classification (ASJC) codes

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title = "Dimethyl 2,2′‐[carbonylbis(Azanediyl)](2s,2′s)‐bis[3‐(4‐hydroxyphenyl)propanoate]",

abstract = "The thus‐far unknown ureic derivative dimethyl 2,2′‐[carbonylbis(azanediyl)](2S,2′S)‐ bis[3‐(4‐hydroxyphenyl)propanoate] has been efficiently synthesized by enantiospecific oxidative carbonylation of readily available L‐tyrosine methyl ester, using a very simple catalytic system (PdI2 in conjunction with KI) under relatively mild conditions (100 °C for 5 h in DME as the solvent and under 20 atm of a 4:1 mixture CO‐air).",

author = "{Palumbo Piccionello}, Antonio and {Della Ca{\textquoteright}}, Nicola and Carla Carfagna and Gioia, {Katia F.} and Bartolo Gabriele and Raffaella Mancuso",

year = "2018",

language = "English",

volume = "2018",

pages = "M983--",

journal = "MolBank",

issn = "1422-8599",

publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",

}

TY - JOUR

T1 - Dimethyl 2,2′‐[carbonylbis(Azanediyl)](2s,2′s)‐bis[3‐(4‐hydroxyphenyl)propanoate]

AU - Palumbo Piccionello, Antonio

AU - Della Ca’, Nicola

AU - Carfagna, Carla

AU - Gioia, Katia F.

AU - Gabriele, Bartolo

AU - Mancuso, Raffaella

PY - 2018

Y1 - 2018

N2 - The thus‐far unknown ureic derivative dimethyl 2,2′‐[carbonylbis(azanediyl)](2S,2′S)‐ bis[3‐(4‐hydroxyphenyl)propanoate] has been efficiently synthesized by enantiospecific oxidative carbonylation of readily available L‐tyrosine methyl ester, using a very simple catalytic system (PdI2 in conjunction with KI) under relatively mild conditions (100 °C for 5 h in DME as the solvent and under 20 atm of a 4:1 mixture CO‐air).

AB - The thus‐far unknown ureic derivative dimethyl 2,2′‐[carbonylbis(azanediyl)](2S,2′S)‐ bis[3‐(4‐hydroxyphenyl)propanoate] has been efficiently synthesized by enantiospecific oxidative carbonylation of readily available L‐tyrosine methyl ester, using a very simple catalytic system (PdI2 in conjunction with KI) under relatively mild conditions (100 °C for 5 h in DME as the solvent and under 20 atm of a 4:1 mixture CO‐air).

UR - http://hdl.handle.net/10447/351038

UR - http://www.mdpi.com/1422-8599/2018/1/M983/pdf

M3 - Article

SN - 1422-8599

VL - 2018

SP - M983-

JO - MolBank

JF - MolBank

ER -

Dimethyl 2,2′‐[carbonylbis(Azanediyl)](2s,2′s)‐bis[3‐(4‐hydroxyphenyl)propanoate]

Abstract

All Science Journal Classification (ASJC) codes

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