Preparation of dendrons with peripheral fullerene units

DOI: 10.1016/S0040-4039(98)02378-8

Source and publish data:

Tetrahedron Letters p. 269 - 272 (1999)

Update date:2022-08-03

Topics: Synthesis Characterization Yield Protecting group Michael addition Purification Conjugation Workup Reaction Monitoring Coupling Reaction Click Chemistry Fullerene Stoichiometry Sonication

Authors:

Nierengarten, Jean-Francois

Felder, Delphine

Nicoud, Jean-Francois

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4039(98)02378-8

Highly soluble dendritic branches with fullerene subunits at the periphery and a carboxylic acid function at the focal point have been prepared by a convergent approach, using successive DCC-mediated esterifications followed by cleavage of a t-butyl ester moiety under acidic conditions.

Full text of DOI:10.1016/S0040-4039(98)02378-8

Products guided by the article

Product name:bis{[3,5-bis(octyloxy)phenyl]methyl} 11''-(carboxymethoxy)-4'',15''-dioxo-3',3''-(methanoxymethano[1,3]benzenomethanoxymethano)-3'H,3''H-dicyclopropa[1,9:3,15][5,6]fullerene-C₆₀-I_h-3',3''-dicarboxylate

Cas No:220791-20-8

R&D Labs maybe for 220791-20-8

SHUNYUANSHENG BIO-PHARMTECH CO., LTD

website:https://www.whsysbio.com

Contact:--

Address:Building 13, Liandong U Valley-Wuhan Economic Innovation Valley, No. 259, Xingsan Road, Shamao Street, Hannan District, Wuhan City, Hubei Province
Chengdu Herbpurify Co., Ltd

website:http://www.herbpurify.com

Contact:0086-028-85249238

Address:Room709-C1,Incubator Building, Tianfu Life Science Park No.88,Keyuan Road,Gaoxin district,Chengdu City,Sichuan Prov,China
Tianjin Ji Ping Jia Chemical Co., Ltd.

Contact:18622448868

Address:tianjin
Shanghai Science Peptide Biological Technology Co.,ltd

website:http://www.scipeptide.com

Contact:+86-21-51099675

Address:No.8 Changyang Rd
Penglai Qianwei Chemical Co., Ltd.

Contact:86-535-3357802

Address:Shahelu (north), Penglai, Shandong, China

Relevant to this article

Hybrid P-chiral diphosphines for asymmetric hydrogenation

Doi:10.1039/a808711c
(1999)
First total synthesis of acerogenin C and aceroside IV

Doi:10.1021/jo9714324
(1997)
Copper(I) mediated highly diastereoselective conjugate addition of Grignard reagents to functionalised cycloalkenols: A general and efficient route for the stereoselective synthesis of 5- and 6-membered ring trisubstituted cycloalkanols

Doi:10.1016/S0040-4020(01)00044-8
(2001)
Cycloadditions of noncomplementary substituted 1,2,3-triazines

Doi:10.1021/ol502436n
(2014)
Doi:10.1016/S0040-4039(01)87511-0
(1969)
Syntheses of nucleosides designed for combinatorial DNA sequencing

Doi:10.1002/(SICI)1521-3765(19990301)5:3<951::AID-CHEM951>3.0.CO;2-G
(1999)

Article Doi