54257-94-2Relevant academic research and scientific papers
Formaldehyde-Extruding Homolytic Aromatic Substitution via C→O Transposition: Selective ‘Traceless-Linker’ access to Congested Biaryl Bonds
Poonpatana, Pabhon,dos Passos Gomes, Gabriel,Hurrle, Thomas,Chardon, Kimhoa,Br?se, Stefan,Masters, Kye-Simeon,Alabugin, Igor
supporting information, p. 9091 - 9097 (2017/07/11)
A new, selective way to form C?C bonds has been developed. In this report, we disclose the homolytic aromatic substitution via C→O transposition coupled with the elimination of formaldehyde (as a traceless linker). Computational analysis indicates the sel
Tethering for selective synthesis of 2,2′-biphenols: The acetal method
Masters, Kye-Simeon,Bihlmeier, Angela,Klopper, Wim,Braese, Stefan
supporting information, p. 17827 - 17835 (2014/01/17)
2,2'-Biphenols are a large and diverse group of compounds with exceptional properties both as ligands and bioactive agents. Traditional methods for their synthesis by oxidative dimerisation are often problematic and lead to mixtures of ortho- and para-connected regioisomers. To compound these issues, an intermolecular dimerisation strategy is often inappropriate for the synthesis of heterodimers. The 'acetal method' provides a solution for these problems: stepwise tethering of two monomeric phenols enables heterodimer synthesis, enforces ortho regioselectivity and allows relatively facile and selective intramolecular reactions to take place. The resulting dibenzo[1,3]dioxepines have been analysed by quantum chemical calculations to obtain information about the activation barrier for ring flip between the enantiomers. Hydrolytic removal of the dioxepine acetal unit revealed the 2,2′-biphenol target. All tied up! Oxidative dimerisation of phenols often results in regioisomeric mixtures. One solution is the use of an acetal tether to impart ortho reactivity to the hydroxyarenes in a 1:1 ratio. Cyclisation forms dibenzo[1,3]dioxepine intermediates, then cleavage of the acetal linker delivers the unmasked biphenol (see scheme). Copyright
The acetal concept: Regioselective access to ortho,ortho-diphenols via dibenzo-1,3-dioxepines
Masters, Kye-Simeon,Br?se, Stefan
, p. 866 - 869 (2013/02/26)
Traditional methods are ill-suited for the synthesis of ortho,ortho-biphenols, a structural motif found in many polyphenolic natural products, as well as synthetically useful compounds such as the chiral ligands binol, vapol, and vanol. The new route consists of a radical-based reaction of an acetal-tethered biphenyl ether substrate and subsequent hydrolytic cleavage of the dibenzo-1,3-dioxepine intermediate. Copyright
Synthesis of hexahydrochromeno[4,3-b]azepine derivatives
Pavé, Grégoire,Léger, Jean-Michel,Jarry, Christian,Viaud-Massuard, Marie-Claude,Guillaumet, Gérald
, p. 4219 - 4222 (2007/10/03)
Synthesis of optically pure (6aR,11aS)-7,8,9,10,11,11a-hexahydro-5-oxa-11- azacyclohepta[a]naphthalen-6a-ylamine from 2-cyano-6-oxazolopiperidine is described via the CN(R,S) strategy. The lithium aluminium hydride involves a one-pot reduction and a ring-
