Coordination Compounds of Substituted 1,10-Phenanthrolines and Related Dipyridyls. I. Synthesis of 2,9-Dimethyl-1,10-phenanthroline

1960 ◽  
Vol 13 (1) ◽  
pp. 145 ◽  
Author(s):  
EJ O'Reilly ◽  
RA Plowman

A direct synthesis of 2,9-dimethyl-1,10-phenanthroline has been developed. The method involves a Skraup type of reaction between o-phenylenediamine, crotonaldehyde, and either arsenic(V) oxide or sodium m-nitrobenzenesulphonate. Some derivatives of 2,9-dimethyl-1,10-phenanthroline have been characterized.

1970 ◽  
Vol 9 (5) ◽  
pp. 1071-1075 ◽  
Author(s):  
William E. Newton ◽  
Eugene G. Rochow

2006 ◽  
Vol 84 (10) ◽  
pp. 1250-1253 ◽  
Author(s):  
Mee-Kyung Chung ◽  
Paul Fancy ◽  
Jeffrey M Stryker

The direct synthesis of sterically hindered, partially etherified derivatives of tetrakis(2-hydroxyphenyl)ethene is reported by using the McMurry reductive olefination reaction on a range of differentially substituted 2,2′-dialkoxy benzophenone substrates. Three orthogonal protection strategies are demonstrated, incorporating β-silylethyl, 3-butenyl, and tert-butyl protecting groups, respectively, into the starting benzophenones. The latter proved most efficient, with both the McMurry coupling and deprotection steps occurring concomitantly under the McMurry conditions to directly yield the desired bis(2-hydroxyphenyl)-bis(2-methoxyphenyl)ethene as a 1:1 mixture of E- and Z-diastereoisomers.Key words: preorganized polyaryloxide ligands, McMurry olefination, titanium trichloride, supramolecular chemistry, tetrakis(2-hydroxyphenyl)ethene, 2,2′-disubstituted benzophenone.


1966 ◽  
Vol 19 (4) ◽  
pp. 539 ◽  
Author(s):  
GE Coates ◽  
C Kowala ◽  
JM Swan

Various triethylphosphine coordinated gold(1) mercaptides of formula Et3PAuSR (R = Me, Et, Pr, Bu, Bu1, Ph, CH2Ph, β-C10H7, and CH2CH(NH2)C02H), and related sulphur derivatives of formula Et3PAuY (Y = SCN, SC(S)Net2, SC(S)OEt, and SC(NH2)NH2+Br-) have been prepared. Under appropriate conditions, displacement of the sulphur group from the gold atom is observed, either by another sulphur nucleophile, e.g. Et3PAuSR + Et2NCSS- → Et3PAuSC(S)Net2 + RS-, or by a. nucleophile such as Cl-, Br-, I-, NO3-, or CN-.


2000 ◽  
Vol 30 (14) ◽  
pp. 2541-2548 ◽  
Author(s):  
Georges Dewynter ◽  
A. Houssem Hajri ◽  
Loic Toupet ◽  
Jean-Louis Montero

1973 ◽  
Vol 12 (6) ◽  
pp. 1453-1454 ◽  
Author(s):  
Joel Wright ◽  
Alexander Kaczmarczyk

Synlett ◽  
2010 ◽  
Vol 2010 (05) ◽  
pp. 721-724
Author(s):  
Parthasarathi Das ◽  
Kintali Sreeramamurthy ◽  
Ettam Ashok ◽  
Velisoju Mahendar ◽  
Gourishetti Santoshkumar

2013 ◽  
Vol 51 (3) ◽  
pp. 586-593 ◽  
Author(s):  
P. Bindu ◽  
Shravan Reddy Naini ◽  
K. Shanmukha Rao ◽  
P. K. Dubey ◽  
Sarbani Pal

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