Results 1 to 10 of about 473 (148)
Palladium‐Catalyzed Cascade to Benzoxepins by Using Vinyl‐Substituted Donor–Acceptor Cyclopropanes [PDF]
A palladium‐catalyzed intermolecular cascade (4+3) cyclocondensation of salicylaldehydes and vinylcyclopropanes is reported. A key feature of the reaction is the use of a phosphonate group as an acceptor moiety on the cyclopropane, exploiting its ...
Matteo Faltracco +2 more
exaly +9 more sources
Benzoxepins (Update 2012) [PDF]
AbstractThis manuscript is an update to the earlier Science of Synthesis contribution describing methods for the synthesis of benzoxepins. It focuses on the literature published in the period 2003–2011.
Li +5 more
core +3 more sources
Aluminum(III)-Promoted Prins Cyclization of 2-Allylphenols: An Expedient Synthesis of Benzoxepins
2-Allylphenols undergo smooth cross coupling with ketones under mild conditions to produce spirocyclic oxepins in good yields with high chemoselectivity, whereas aromatic aldehydes provide benzoxepins with moderate stereoselectivity.
Nagendra Nath Yadav
exaly +3 more sources
ChemInform Abstract: THE SYNTHESIS OF 1-HALOALKYL-1,3,4,5-TETRAHYDRO-2-BENZOXEPINS
AbstractDie Reduktion der Phenylpropionsäure (Ia) liefert das Carbinol (Ib), das zum Acetal (II) substituiert und dann zum Brommethyl‐benzoxepin (III) cyclisiert wird.
TENBRINK
core +3 more sources
AbstractFor Abstract see ChemInform Abstract in Full Text.
von Angerer
core +2 more sources
The 4-phenyl-l-benzoxepins 4, 5 and 8 have been prepared from the seven-membered diketone 1 by enol-alkylation or -acylation reactions; their photoreaction yields the corresponding 1-phenyl-2a,7 b-dihydrocyclobuta[b] l-benzofurans 9, 10 and 11.
H. Hofmann, R. Heidrich, A. Seubert
exaly +2 more sources
Two unprecedented benzoxepins were obtained from the ethyl acetate fraction of the leaves of Rhizophora annamalayana Kathir, and characterized as 4-(11-(hydroxymethyl)-10-methylpentan-2-yl)-4, 5-dihydrobenzo[c]oxepin-1(3H)-one (1) and (E)-methyl-14 ...
Kajal Chakraborty +3 more
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ChemInform Abstract: 3‐Methyl‐2,5‐dihydro‐1‐benzoxepins and 3‐Methyl‐2,5‐dihydrooxepins.
Three preparative procedures of seven-membered O-heterocyclic 3-methyl-2,5-dihydro-l-benzoxepin derivatives are summarized. For the Z-selective formation of C=C double bond, the first approach used the Grubbs ring-closing methathesis, the second approach
Seiji Yamaguchi
core +2 more sources

