- Asymmetric Dieckmann condensation via memory of chirality: synthesis of the key intermediate for AS-3201, an aldose reductase inhibitor.
[作者:Watanabe, Toshihide;Kawabata, Takeo;,期刊:Heterocycles, 页码:1593-1606 , 文章类型: 研究论文,,卷期:2008年76-2]
- Asym. Dieckmann condensation via memory of chirality was developed. A key intermediate, succinimide I, for the synthesis of AS-3201, an aldose reductase inhibitor, was prepd. in 94% ee by asym. Dieckmann condensation of...
- Asymmetric hetero Diels-Alder reaction of nitroso compounds utilizing tartaric acid ester as a chiral auxiliary.
[作者:Sakai, Hiroki;Ding, Xia;Yoshida, Tetsusuke;Fujinami, Shuhei;Ukaji, Yutaka;Inomata, Katsuhiko;,期刊:Heterocycles, 页码:1285-1300 , 文章类型: 研究论文,,卷期:2008年76-2]
- The regio- and enantioselective hetero Diels-Alder reaction of a nitroso compd. with a cyclic dienol, cyclohexa-1,3-dienemethanol, was realized utilizing a stoichiometric amt. of tartrate as a chiral auxiliary to afford ...
- Synthesis, structure, and properties of 2,5,8,11,14,17-hexamethyltriphenyleno[2,1-b:3,4-b':6,5-b'':7,8-b''':10,9- b'''':11,12-b''''']hexathiophene.
[作者:Endou, Masaru;Ie, Yutaka;Aso, Yoshio;,期刊:Heterocycles, 页码:1043-1048 , 文章类型: 研究论文,,卷期:2008年76-2]
- b'''':11,12-b''''']hexathiophene I was synthesized by Fe(III)-mediated oxidative cyclization of hexakis(2-methyl-4-thienyl)benzene, and its structure was detd. by x-ray crystallog. anal. [triclinic, space group P-1, a 8....
- Free radical tandem addition-cyclization of Te-phenyl N,N-dimethylcarbamotelluroate to 1,6-enynes.
[作者:Fujiwara, Shin-ichi;Shimizu, Yoshihiko;Makita, Yoshimasa;Shin-ike, Tsutomu;Kambe, Nobuaki;,期刊:Heterocycles, 页码:1577-1584 , 文章类型: 研究论文,,卷期:2008年76-2]
- Radical tandem addn. of Me2NC(O)TePh (I) to alkenes and alkynes was examd. Simple addn. of I to alkenes such as styrene and acrylate did not take place under irradn. of visible light. However, when alkynes were added t...
- Novel substituted tetrathia[7]helicenes by direct functionalization of the helical system or photocyclization of substituted 1,2-(bis-benzodithienyl)ethenes.
[作者:Rigamonti, Clara;Ticozzelli, Maria Teresa;Bossi, Alberto;Licandro, Emanuela;Giannini, Clelia;Maiorana, Stefano;,期刊:Heterocycles, 页码:1439-1470 , 文章类型: 研究论文,,卷期:2008年76-2]
- The synthesis of several tetrathia[7]helicenes functionalized with different electron-donor and electron-acceptor substituents in the positions 2,13 (the a positions of terminal thiophene rings) and/or 7,8 (on the centra...
- Influence of the position of tert-butyl substituents on reactivity of quinone dimers yielding dibenzofuran-1,4-diones.
[作者:Hayashi, Naoto;Kanda, Akifumi;Higuchi, Hiroyuki;Ninomiya, Keiko;,期刊:Heterocycles, 页码:1361-1367 , 文章类型: 研究论文,,卷期:2008年76-2]
- Reactivity of two isomeric quinone dimers, 5,5'- (I) and 6,6'-di-tert-butyl-2,2'-bisbenzoquinone (II) were compared. Both quinone dimers underwent thermal cyclization in EtOH to give dibenzofuran-1,4-diones exclusively,...
- Epimerization of trans-3-arylaziridine-2-carboxylates at the C3 position.
[作者:Kumamoto, Takuya;Nagayama, Shiin-ichiro;Hayashi, Yukiko;Kojima, Hiroaki;David, Lemin;Nakanishi, Waka;Ishikawa, Tsutomu;,期刊:Heterocycles, 页码:1155-1170 , 文章类型: 研究论文,,卷期:2008年76-2]
- An effective trans to cis epimerization of 1-benzyl-3-arylaziridine-2-carboxylates is described. The combination of Sm metal, I2, and Me2N(CH2)2OH promoted the epimerization of the trans isomer to a cis and trans mixt. ...
- Synthesis of substituted aziridines via intramolecular reactions of b-N-chloroethylamino carbanions.
[作者:Makosza, Mieczyslaw;Bobryk, Karolina;Krajewski, Dariusz;,期刊:Heterocycles, 页码:1511-1524 , 文章类型: 研究论文,,卷期:2008年76-2]
- Simple and efficient method of synthesis of 2-alkoxycarbonyl-, 2-cyano-, and 2-phenylsulfonyl-N-alkylaziridines was elaborated via intramol. nucleophilic substitution of Cl in N-chloro-2-alkoxycarbonyl(cyano, phenylsulfo...
- A convenient synthesis of optically active biopterin.
[作者:Shiro, Yuichi;Urano, Fumi;Kuroda, Yasuhiro;Murata, Shizuaki;,期刊:Heterocycles, 页码:1329-1335 , 文章类型: 研究论文,,卷期:2008年76-2]
- Naturally occurring L-erythro-biopterin is synthesized using regioselective pteridine-ring formation from a chiral a,b-epoxy aldehyde intermediate, which is prepd. from L-lactate via Sharpless epoxidn.
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