127-06-0 = 79-46-9 反应条件:1.1 Reagents: Triisopropanolamine,Tetrapropylammonium Hydroxide,Hydrogen Peroxide Solvents: Methanol; 1.5 H,70 °C 标题:Green Synthesis Of 2-Nitropropane Via Ammoximation-Oxidation Over Organic Base Modified Ts-1 Catalysts 作者:Zhang,Zhiqiang; Chu,Qingyan; Sun,Yuan; Wang,Hao; Lu,Deming; Et Al 参考文献:Chemistryselect 日期:2022 卷标:7(35)]
= 79-46-9 反应条件:1.1 Reagents: Nitrogen Dioxide Catalysts: N-Hydroxyphthalimide Solvents: (Trifluoromethyl)Benzene 标题:An Efficient Nitration Of Light Alkanes And The Alkyl Side-Chain Of Aromatic Compounds With Nitrogen Dioxide And Nitric Acid Catalyzed By N-Hydroxyphthalimide 作者:Nishiwaki,Yoshiki; Sakaguchi,Satoshi; Ishii,Yasutaka 参考文献:Journal Of Organic Chemistry 日期:2002 卷标:67(16) 页码:5663-5668]
= 79-46-9 反应条件:1.1 Reagents: Iodoethane,Pyridine,4-Ethenyl-,Polymer With Diethenylbenzene,Compd. With Iodoethane (Nitrite Anion-Exchanged) Solvents: Acetonitrile; 24 H,Rt1.2 Reagents: Sodium Nitrite Solvents: Water; 24 H,Rt1.3 Solvents: Hexane; 72 H,Rt 标题:Synthesis Of Nitroalkanes From Alkyl Halides Under Mild And Nonaqueous Conditions By Using Polymer Supported Nitrites 作者:Zarchi,Mohammad Ali Karimi; Zarei,Amin 参考文献:Journal Of The Chinese Chemical Society (Taipei 日期:2005 卷标:52(2) 页码:309-311]
41774-06-5 = 79-46-9 反应条件:1.1 Solvents: Dimethylformamide 标题:Desulfonylation Of α-Nitrosulfones With N-Benzyl-1,4-Dihydronicotinamide 作者:Ono,Noboru; Tamura,Rui; Tanikaga,Rikuhei; Kaji,Aritsune 参考文献:Journal Of The Chemical Society 日期:1981 卷标:(3) 页码:71-2]
594-71-8 = 79-46-9 反应条件:1.1 Reagents: Tributylstannane Solvents: Benzene-D6; 14.5 H 标题:Free-Radical Clocks In The Aliphatic Srn1 Process And Reactions Of Nucleophiles With 1,1-Dinitro-2,2-Diphenylethylene 作者:Dedolph,Douglas Frederick 参考文献:1983]
专利号:US-5442065-A 优先权日:1993-09-09 标 题:Synthesis of tetrahydroquinoline enediyne core analogs of dynemicin 发明人:MAGNUS PHILIP D; ILIADIS THEODORE; EISENBEIS SHANE A; FAIRHURST ROBIN A 权利人:UNIV TEXAS 摘要:A process is described for the preparation of the core azobicyclo[7.3.1]tridecaenediyne moiety of the antitumor antibiotic dynemicin. The synthesis allows efficient production of the enediyne as a stable, compound in good yield from the adamantyl N-protected azabicyclo[7.3.1]tridecadiyne. The adamantyl protecting group is employed in the starting material, N-adamantyl dihydroquinoline or N-adamantyl 6-methoxy quinoline. Also disclosed are process for the synthesis of 3-hydroxy-6-methoxyquinoline and several N-substituted derivatives of azobicyclo[7.3.1]tridecaenediyne. Solid tumor and leukemia assays were performed on the analogs of dynemicin. The results suggest a method that these compounds will useful in treating certain types of leukemias and solid tumors. The disclosed synthesis provides a route to new dynemicin intermediates and analogs which will allow development of second and third generation dynemicins.
专利号:US-10633360-B2 优先权日:2014-12-23 标题 :Efficient process for the synthesis of alkoxy substituted benzaldehydes 发明人:MOHAPATRA Manoj Kumar; BENDAPUDI Ramamohanrao; MENACHERRY Paul Vincent; PAUL VINCENT 权利人:ANTHEA AROMATICS PRIVATE LTD 摘要:The present invention relates to the synthesis of alkoxy substituted benzaldehydes obtained from the corresponding alkoxy substituted benzenes. Alkoxy substituted benzaldehydes are products of broad commercial interest and are used as end products and intermediates in flavor and fragrance applications and pharmaceutical ingredients. For example, 3,4-methylendioxy-benzaldehyde (also known as heliotropin or piperonal) is used widely both as a end product and intermediate for the above mentioned applications. Other examples include 3,4-dimethoxybenzaldehyde, 3,4,5-trimethoxybenzaldehyde and 3,4-ethylenedioxybenzene which are intermediates in the synthesis of active pharmaceutical intermediates.
专利号:US-4219489-A 优先权日:1978-09-05 标题:Synthesis of steroids 发明人:BUNES LEONARD A; JOHNSON WILLIAM S 权利人:STANFORD LELAND JUNIOR UNIV TR 摘要:Method and compounds are provided for use in the synthesis of steroids wherein a polyolefin is provided having an initiating group having a chalcogen atom in juxtaposition to a double bond, so as to be capable of bond formation to close to form a ring and having a terminating group involving pi unsaturation (a double or triple bond) conjugated to an aromatic ring. Upon acid catalysis, sigma bonds are formed through the interaction of a carbocation formed at the carbon atom bonded to the chalcogen atom and the double bond intermediate the initiating group and the terminating group, which close to form rings of a steroid nucleus, the carbocation interacting with the pi unsaturation conjugated with the aromatic group and being captured by a nucleophile present in the acidic reaction medium. The resulting steroid product may then be modified in known ways to produce known steroids.
专利号:US-12281398-B2 优先权日:2022-02-07 标题:Microfluidic process for the general electrochemical synthesis of geminal dipseudohalide or halide-pseudohalide compounds 发明人:SCHROER THORSTEN G; LECROY GREGORY E; AGUILA MIGUEL; RODRIGUEZ MAYRA P; DOWNARD TYLER J; MACLEOD BRIANNA L 权利人:US GOV AIR FORCE; US AIR FORCE 摘要:A process for the microfluidic electrochemical synthesis of geminal dipseudohalide or halide-pseudohalide compounds comprising the steps ofpumping a solution comprising a compound of Formula Iinto a microfluidic electrochemical reactor in the presence of a base, one of a halide or pseudohalide salt (MY), and a mediator;applying an electrical current through the microfluidic electrochemical reactor; andperforming oxidative addition to create a geminal dipseudohalide or halide-pseudohalide compound of the general Formula II
专利号:US-3884945-A 优先权日:1973-04-26 标题 :Synthesis of steroids by cyclization in nitro solvents 发明人:JOHNSON WILLIAM S; MORTON DOUGLAS R; GRAVESTOCK MICHAEL B 权利人:UNIV LELAND STANFORD JUNIOR 摘要:Synthesis of steroids by cyclization of a dienyne cyclization substrate to a steroid or A-nor steroid employing a primary or secondary aliphatic nitro compound as solvent, thereby forming an oxime ether group at the C-17 position of the resulting steroid (or at the corresponding position of the resulting A-nor steroid where that is the product of cyclization). This oxime group can be converted to an hydroxy group by reductive cleavage. Conversion of the cyclization products to steroids such as 17hydroxypregnan-20-ones and testosterone is facilitated. The method is also applied to cyclization of suitable substrates to bicyclic products.
专利号:US-4866175-A 优先权日:1966-11-08 标 题 :Novel process for the synthesis of quinoxaline and benzimidazole-N-oxides 发明人:ISSIDORIDES COSTAS H; HADDADIN MAKHLUF J 权利人:RESEARCH CORP 摘要:The synthesis of quinoxaline and benzimidazole-N-oxides and of ester amd amide derivatives of 3-hydroxy-2-quinoxalinecarboxylic acid by a movel process consisting of the reaction between a benzofuroxan and an activated methylene-containing compound under basic conditions.