Synthesis of 2,5-disubstituted 1,3,4-oxadiazoles containing a sterically hindered 4-hydroxy-3,5-di(tert-butyl)phenyl group

1997 ◽  
Vol 33 (6) ◽  
pp. 718-723
Author(s):  
V. I. Kelarev ◽  
V. N. Koshelev ◽  
M. A. Silin
Keyword(s):  
Phenyl Group ◽  
Tert Butyl ◽  
Sterically Hindered

New sterically hindered bis-catechol, bis- o -quinone and its bis-triphenylantimony(v) bis-catecholate. 3,5-Di- tert -butyl-6-methoxymethylcatechol as alkylating agent

2018 ◽  
Vol 28 (1) ◽  
pp. 76-78 ◽  
Author(s):  
Maxim V. Arsenyev ◽  
Tatyana V. Astafeva ◽  
Evgeny V. Baranov ◽  
Andrey I. Poddelsky ◽  
Sergey A. Chesnokov
Keyword(s):  
Alkylating Agent ◽  
Tert Butyl ◽  
Sterically Hindered

Bis(ether) derivatives of tetrakis(2-hydroxyphenyl)ethene — Direct synthesis of (E)- and (Z)-bis(2-hydroxyphenyl)-bis(2-methoxyphenyl)ethene via the McMurry olefination reaction

2006 ◽  
Vol 84 (10) ◽  
pp. 1250-1253 ◽  
Author(s):  
Mee-Kyung Chung ◽  
Paul Fancy ◽  
Jeffrey M Stryker
Keyword(s):  
Supramolecular Chemistry ◽  
Direct Synthesis ◽  
Protecting Groups ◽  
Tert Butyl ◽  
Orthogonal Protection ◽  
Protection Strategies ◽  
Titanium Trichloride ◽  
Sterically Hindered ◽  
Derivatives Of

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.

A new sterically hindered asymmetric zinc phthalocyanine as an efficient sensitizer for dye-sensitized solar cells

2021 ◽  
Author(s):  
Kevser Harmandar ◽  
Kevin Granados-Tavera ◽  
Merve Keskin ◽  
Mehmet Nebioğlu ◽  
İlkay Şişman ◽  
...  
Keyword(s):  
Solar Cells ◽  
Carboxylic Acid ◽  
Dye Sensitized Solar Cells ◽  
Zinc Phthalocyanine ◽  
Tert Butyl ◽  
Dye Sensitized ◽  
Anchoring Group ◽  
Sterically Hindered ◽  
Sensitized Solar Cells

An asymmetric zinc phthalocyanine dye (KH1) bearing three 2,6-di-tert-butyl-4-methylphenoxy donor groups and carboxylic acid anchoring group was synthesized as a sensitizer for dye-sensitized solar cells (DSSCs). The DSSC based on...

Interaction of 3,5-di-tert-butyl-o-benzoquinone with secondary amines—a pathway to new sterically hindered N,N-disubstituted o-aminophenols

Tetrahedron ◽  
2011 ◽  
Vol 67 (1) ◽  
pp. 80-84 ◽  
Author(s):  
Vladimir Cherkasov ◽  
Nikolay Druzhkov ◽  
Tatiana Kocherova ◽  
Georgii Fukin ◽  
Andrey Shavyrin
Keyword(s):  
Secondary Amines ◽  
Tert Butyl ◽  
Sterically Hindered
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