Diastereoselective Ugi reaction without chiral amines: the synthesis of chiral pyrroloketopiperazines
暂无分享,去创建一个
[1] M. Mironov. Design of Multi‐Component Reactions: From Libraries of Compounds to Libraries of Reactions , 2006 .
[2] Alexander Dömling,et al. Recent developments in isocyanide based multicomponent reactions in applied chemistry. , 2006, Chemical reviews.
[3] S. Sollis. Short and novel stereospecific synthesis of trisubstituted 2,5-diketopiperazines. , 2005, The Journal of organic chemistry.
[4] Andrea Basso,et al. A novel highly selective chiral auxiliary for the asymmetric synthesis of L- and D-alpha-amino acid derivatives via a multicomponent Ugi reaction. , 2005, The Journal of organic chemistry.
[5] Alexey P. Ilyn,et al. AN EFFICIENT SYNTHESIS OF 3-OXO-1,2,3,4-TETRAHYDROPYRROLO[1,2-α]PYRAZINE-1-CARBOXAMIDES USING NOVEL MODIFICATION OF UGI CONDENSATION , 2005 .
[6] Jieping Zhu. Recent Developments in the Isonitrile‐Based Multicomponent Synthesis of Heterocycles , 2003 .
[7] I. Ugi,et al. Stereoselective U-4CRS with 1-amino-5-desoxy-5-thio-2,3,4-O-isobutanoyl-β-d-xylopyranose: an effective and selectively removable chiral auxiliary , 2002 .
[8] R. Nutt,et al. Concise total synthesis of the prolyl endopeptidase inhibitor eurystatin A via a novel Passerini reaction–deprotection–acyl migration strategy , 2001 .
[9] C. Willis,et al. Ugi four component condensations using aldehydes with an asymmetric centre at C-2 , 2000 .
[10] I. Ugi,et al. Multicomponent Reactions with Isocyanides. , 2000, Angewandte Chemie.
[11] T. Ziegler,et al. PASSERINI AND UGI REACTIONS OF BENZYL AND ACETYL PROTECTED ISOCYANOGLUCOSES , 1999 .
[12] W. Herlihy,et al. Unique Structures Generated by Ugi 3CC Reactions Using Bifunctional Starting Materials Containing Aldehyde and Carboxylic Acid. , 1999, The Journal of organic chemistry.
[13] M. Murata,et al. Novel, highly potent aldose reductase inhibitors: (R)-(-)-2-(4-bromo-2-fluorobenzyl)-1,2,3,4- tetrahydropyrrolo[1,2-a]pyrazine -4-spiro-3'-pyrrolidine-1,2',3,5'-tetrone (AS-3201) and its congeners. , 1998, Journal of medicinal chemistry.
[14] T. Ziegler,et al. PASSERINI AND UGI REACTIONS OF ANOMERIC GLUCOSYL ISONITRILES , 1998 .
[15] H. Kunz,et al. Asymmetric synthesis on carbohydrate templates: stereoselective Ugi-synthesis of .alpha.-amino acid derivatives , 1988 .
[16] H. Kunz,et al. Diastereoselective Strecker Synthesis of α‐Aminonitriles on Carbohydrate Templates , 1987 .
[17] T. Chan,et al. 1,4-Dichloro-1,4-dimethoxybutane as a mild reagent for the conversion of primary amines to pyrroles. Synthesis of a pyrrole compound from tobacco , 1983 .
[18] G. Olah,et al. Synthetic methods and reactions. 62. Transformations with chlorotrimethylsilane/sodium iodide, a convenient in situ iodotrimethylsilane reagent , 1979 .
[19] R. C. Erickson,et al. Semisynthetic cephalosporins. Synthesis and structure-activity relationships of 7-(1-pyrryl)- and 7-(1-indolyl)acetamidocephalosporin derivatives. , 1978, Journal of medicinal chemistry.
[20] I. Ugi,et al. Stereoselective syntheses. V. Isonitriles. XXIV. Stereoselective four-component condensations of .alpha.-ferrocenylethylamine and its absolute configuration , 1970 .
[21] I. Ugi,et al. Stereoselektive Synthesen, III. Die Umsetzung von (S)‐α‐Phenyläthylamin und Isobutyraldehyd mit Benzoesäure und tert.‐Butyl‐isocyanid als Modellreaktion für stereoselektive Peptid‐Synthesen mittels Vierkomponenten‐Kondensationen , 1967 .
[22] Ivar Ugi,et al. Stereoselektive Synthesen, IV. Der Reaktionsmechanismus stereoselektiver Vierkomponenten‐Kondensationen , 1967 .