ChemInform Abstract: On the Reaction of Sterically Hindered α,β-Unsaturated Ketones with Hydroxylamine: Preparation of 5-Hydroxy Derivatives of Isoxazolidine and 4,5-Dihydroisoxazole.

ChemInform ◽  
2013 ◽  
Vol 44 (21) ◽  
pp. no-no
Author(s):  
M. V. Mavrov ◽  
S. I. Firgang
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.


ChemInform ◽  
2011 ◽  
Vol 42 (17) ◽  
pp. no-no
Author(s):  
R. Janciene ◽  
Z. Stumbreviciute ◽  
A. Vektariene ◽  
R. Sirutkaitis ◽  
D. Podeniene ◽  
...  

1997 ◽  
Vol 62 (19) ◽  
pp. 6524-6528 ◽  
Author(s):  
Andrzej Rajca ◽  
Suchada Rajca ◽  
Shailesh R. Desai ◽  
Victor W. Day

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