ChemInform Abstract: Studies on Organometallic Compounds. Part 7. Reaction of Di-tert-butyl Dicarbonate with α-Trialkylstannyl Derivatives of Pyridine, Quinoline, and Isoquinoline.

ChemInform ◽  
2010 ◽  
Vol 26 (48) ◽  
pp. no-no
Author(s):  
Y. YAMAMOTO ◽  
H. OUCHI ◽  
T. TANAKA
2007 ◽  
Vol 60 (1-2) ◽  
pp. 193-196 ◽  
Author(s):  
Abdelwaheb Hamdi ◽  
Rym Abidi ◽  
Jacques Vicens

2006 ◽  
Vol 76 (11) ◽  
pp. 1753-1756 ◽  
Author(s):  
A. A. Prishchenko ◽  
M. V. Livantsov ◽  
O. P. Novikova ◽  
L. I. Livantsova ◽  
D. B. Shpakovskii ◽  
...  
Keyword(s):  

2013 ◽  
Vol 87 (8) ◽  
pp. 1253-1258
Author(s):  
Yu. P. Pavlovskii ◽  
N. S. Kachurina ◽  
S. I. Gerasimchuk ◽  
Yu. Ya. Van-Chin-Syan

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.


2018 ◽  
Vol 120 ◽  
pp. S90-S91
Author(s):  
Alena Kavalenka ◽  
Galina Semenkova ◽  
Ivan Zholnerevich ◽  
Galina Ksendzova ◽  
Victor Sorokin ◽  
...  

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