专利号:US-4891442-A 优先权日:1987-03-09 标 题 :Process for synthesis of β-phenylalanine 发明人:LIN JIANG-JEN; KNIFTON JOHN F 权利人:TEXACO INC 摘要:N-acetyl-β-phenylalanine is synthesized by reacting phenylacetaldehyde, acetamide and synthesis gas with a catalyst comprising a cobalt-containing compound in conjunction with a cocatalyst that may be either a Group VB or VIB containing ligand, or a rhodium compound optionally bonded to one or more Group VB or VIB donor ligands, at a temperature of at least 50° C. and a pressure of at least 500 psi.
专利号:US-8257931-B2 优先权日:2005-01-21 标题 :Regulation of protein synthesis 发明人:WAGNER GERHARD; CHOREV MICHAEL; MOERKE NATHAN JOHN; AKTAS BERTAL HUSEYIN; HALPERIN JOSE 权利人:WAGNER GERHARD; CHOREV MICHAEL; MOERKE NATHAN JOHN; AKTAS BERTAL HUSEYIN; HALPERIN JOSE; HARVARD COLLEGE 摘要:A composition and method for inhibiting proliferation of a tumor cell compared to a non-tumor cell. Also described are methods of screening for a composition that inhibits cap-dependent translation compared to cap-independent translation of proteins.
专利号:CA-1296356-C 优先权日:1987-03-09 标题 :PROCESS FOR SYNTHESIS OF .beta.-PHENYLALANINE
专利号:EP-0281707-A2 优先权日:1987-03-09 标题 :Process for synthesis of beta-phenylalanine
专利号:US-2005113397-A1 优先权日:2002-01-31 标题:Imidazo[1,2-a]pyridine derivative 发明人:TAKEMURA MAKOTO; TAKAHASHI HISASHI; KAWAKAMI KATSUHIRO; TAKESHITA HIROSHI; KIMURA YOUICHI; WATANABE JUN; SUGIMOTO YUICHI; KITAMURA AKIHIRO; NAKAJIMA RYOHEI; KANAI KAZUO; FUJISAWA TETSUNORI 摘要:A compound reprsented by the following formula (I), its salts or nsolvates thereof capable of specifically or selectively expressig an antifungal activity in a broad spectrum based on the novel mechanism thereof of 1,6-β-glucan synthesis inhibition, and an antifungal agent containing any of them.
专利号:US-2007191395-A1 优先权日:2004-02-16 标题 :Heterocyclic compounds having antifungal activity 发明人:KAWAKAMI KATSUHIRO; KANAI KAZUO; FUJISAWA TETSUNORI; MORITA CHIKANORI; SUZUKI TAKASHI 权利人:KAWAKAMI KATSUHIRO; KANAI KAZUO; FUJISAWA TETSUNORI; MORITA CHIKANORI; SUZUKI TAKASHI 摘要:A compound which can specifically or selectively expresses an antifungal activity with a broad spectrum, based on the functional mechanism of 1,6-β-glucan synthesis inhibition, is provided, and an antifungal agent which comprises such a compound, a salt thereof or a solvate thereof is provided. A compound represented by the following formula (I), a salt thereof or a solvate thereof.
参考标题:Synthesis Of A Novel Library Of 1-Substituted Pyrido[1,2-A]Benzimidazoles 作者:Satyanarayana Gadde,Yun Cheuk Leung,Mohan Bhadbade,Belamy B. Cheung,David Stc. Black,Naresh Kumar 摘要:The Reactivity And Synthesis Of New Analogues Of Pyrido[1,2-A]Benzimidazoles Have Been Explored. Twenty-Three Derivatives Bearing Phenoxy, Thiophenoxy, Aniline, And Aryl Groups At The 1-Position Were Successfully Synthesised In 25-91 % Yield, Via Nucleophilic Substitution, Buchwald-Hartwig Amination, And Suzuki Coupling Type Processes. Solvent Free Synthetic Protocols Were Employed To Achieve The Nucleophilic
合成参考文献
参考文献:10.1107/s1600536811018095 摘要:Manickkam V, Kalaivani D, Rajeswari S. Triethyl-ammonium [2-eth-oxy-carbonyl-2-(2-methyl-benz-yl)-6,9-dinitro-3-oxo-bicyclo-[3.3.1]non-6-en-8-yl-idene]azinate. Acta Crystallogr Sect E Struct Rep Online. 2011 Jun 01;67(Pt 6):o1469.