Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Hidehiro Arai"'
Autor:
Hidehiro Arai, Koichiro Morihira, Yusuke Nakamura, Yasuhiro Kataoka, Yoshiaki Horiguchi, Isao Kuwajima
Publikováno v:
ChemInform. 24
Lewis acid-mediated intramolecular cyclization of the dienol silyl ether or enol silyl ether and the acetal for medium-sized ring formation is described. Seven-, eight-, and nine-membered ring cyclization proceed in fairly good yields.
Publikováno v:
ChemInform. 31
Optically active novel 18-demethyltaxiods were successfully synthesized from 2α,10β-dibenzyloxy-11β-(t-butyldimethylsiloxy)-7β-hydroxy-1α-(p-methoxybenzyloxy)-8β,15,15-trimethyl-4-methylene-trans-bicyclo[6.4.0]dodecan-9-one (2) which correspond
Publikováno v:
ChemInform. 32
Unsymmetrical alkyl 2-hydroxy-1-(1-hydroxyalkyl)alkyl ketones (bis-aldols) are successfully synthesized by way of sequential two aldol reactions using α-bromo ketones and two different aldehydes. In the first reaction, α-bromo-β-stannyloxy ketones
Publikováno v:
ChemInform. 33
Methyl 1,2-dialkoxy-11,11-dimethyl-9-oxobicyclo[5.3.1]-undec-7-en-8-carboxylate 19 was synthesized by cesium fluoride-mediated intramolecular Knoevenagel reaction of methyl 4-(1,8-dialkoxy-2,2-dimethyl-3-oxocyclooctyl)-3-oxobutanonate 18.
Autor:
Hidehiro Arai, Yasuhiro Kataoka, Isao Kuwajima, Yusuke Nakamura, Yoshiaki Horiguchi, Koichiro Morihira
Publikováno v:
Tetrahedron Letters. 33:6979-6982
Lewis acid-mediated intramolecular cyclization of the dienol silyl ether or enol silyl ether and the acetal for medium-sized ring formation is described. Seven-, eight-, and nine-membered ring cyclization proceed in fairly good yields.
Publikováno v:
ChemInform. 34
Double aldol reaction proceeded stereoselectively at one α-carbon of ketones to give α-(1-hydroxyalkyl)-β-hydroxyalkyl ketones (double aldols) in good to high yields by the following three methods: i) tin(II) trifluoromethanesulfonate-mediated ald
Publikováno v:
ChemInform. 31
Unsymmetrical alkyl or aryl 2-hydroxy-1-(1-hydroxyalkyl)alkyl ketones (bis-aldols) were synthesized by the samarium(II) iodide-mediated aldol reaction of aldehydes with alkyl or aryl oxiranyl ketones. Bis-aldols were formed via the aldol reaction of
Publikováno v:
Chemistry Letters. 31:92-93
Methyl 1,2-dialkoxy-11,11-dimethyl-9-oxobicyclo[5.3.1]-undec-7-en-8-carboxylate 19 was synthesized by cesium fluoride-mediated intramolecular Knoevenagel reaction of methyl 4-(1,8-dialkoxy-2,2-dimethyl-3-oxocyclooctyl)-3-oxobutanonate 18.
Publikováno v:
Chemistry Letters. 31:82-83
A polyoxy eight-membered ring compound containing a bis-aldol skeleton, 2,6-dibenzyloxy-3-(t-butyldimethylsiloxy)-7-hydroxy-8-hydroxymethyl-5-(p-methoxybenzyloxy)-4,4-dimethylcyclooctanone 1, a key synthetic intermediate of 19-hydroxypaclitaxel, was
Publikováno v:
Chemistry Letters. 30:118-119
Unsymmetrical alkyl 2-hydroxy-1-(1-hydroxyalkyl)alkyl ketones (bis-aldols) are successfully synthesized by way of sequential two aldol reactions using α-bromo ketones and two different aldehydes. In the first reaction, α-bromo-β-stannyloxy ketones