109-94-4 + 1826-67-1 = 922-65-6 反应条件:1.1 Solvents: Tetrahydrofuran; 1 H,5 - 15 °C; 1 H,Rt1.2 Reagents: Ammonium Chloride Solvents: Water 标题:Preparation Of 6,8,10-Undecatriene-4-One And Perfume Composition 参考文献:Japan]
109-94-4 + 1826-67-1 = 922-65-6 反应条件:1.1 Solvents: Tetrahydrofuran; 1 H,5 - 15 °C; 1 H,Rt1.2 Reagents: Ammonium Chloride Solvents: Water 标题:Preparation Of 6,8,10-Undeca-Triene-3-One And Perfume Composition 参考文献:Japan]
= 922-65-6 反应条件:1.1 Reagents: Magnesium Catalysts: Iodine Solvents: Tetrahydrofuran; 40 °C1.2 Solvents: Tetrahydrofuran; Reflux; 1 H,Reflux; Reflux -> 0 °C1.3 0 °C; 0 °C -> 23 °C; 2 H,23 °C; 23 °C -> -20 °C1.4 Reagents: Hydrochloric Acid Solvents: Water 标题:Enantioselective Total Synthesis Of Pladienolide B: A Potent Spliceosome Inhibitor 作者:Ghosh,Arun K.; Anderson,David D. 参考文献:Organic Letters 日期:2012 卷标:14(18) 页码:4730-4733]
1826-67-1 = 922-65-6 反应条件:1.1 0 °C; 3 H,Rt1.2 Reagents: Hydrochloric Acid Solvents: Water 标题:Construction Of Silicon-Containing Seven-Membered Rings By Catalytic [4 + 2 + 1] Cycloaddition Through Rhodium Silylenoid 作者:Sasaki,Ikuo; Ohmura,Toshimichi; Suginome,Michinori 参考文献:Organic Letters 日期:2020 卷标:22(8) 页码:2961-2966]
1826-67-1 = 922-65-6 反应条件:1.1 Solvents: Tetrahydrofuran; 15 Min,0 °C; 0 °C -> Rt; 1 - 3 H,Rt1.2 Reagents: Ammonium Chloride Solvents: Water 标题:A Cu/pd Cooperative Catalysis For Enantioselective Allylboration Of Alkenes 作者:Jia,Tao; Cao,Peng; Wang,Bing; Lou,Yazhou; Yin,Xuemei; Et Al 参考文献:Journal Of The American Chemical Society 日期:2015 卷标:137(43) 页码:13760-13763]
62418-65-9 = 922-65-6 反应条件:1.1 Reagents: Selectfluor Solvents: Acetonitrile; 3 Min,150 °C 标题:A Novel,Chemoselective And Efficient Microwave-Assisted Deprotection Of Silyl Ethers With Selectfluor 作者:Shah,Syed Tasadaque A.; Singh,Surendra; Guiry,Patrick J. 参考文献:Journal Of Organic Chemistry 日期:2009 卷标:74(5) 页码:2179-2182]
62418-65-9 = 922-65-6 反应条件:1.1 Catalysts: Bromotrimethylsilane Solvents: Methanol; 5 Min,Rt1.2 Reagents: Sodium Bicarbonate Solvents: Water; Rt 标题:The Chemoselective And Efficient Deprotection Of Silyl Ethers Using Trimethylsilyl Bromide 作者:Shah,Syed Tasadaque A.; Guiry,Patrick J. 参考文献:Organic & Biomolecular Chemistry 日期:2008 卷标:6(12) 页码:2168-2172]
= 922-65-6 反应条件:1.1 Reagents: Magnesium Solvents: Diethyl Ether,Tetrahydrofuran 标题:An Efficient Synthesis Of Functionalized Tricyclo[6.3.1.01.6]Dodec-4-Enes By A Stereoselective Intramolecular Diels-Alder Reaction 作者:Shishido,Kozo; Hiroya,Kou; Ueno,Yutaka; Fukumoto,Keiichiro; Kametani,Tetsuji; Et Al 参考文献:Journal Of The Chemical Society 日期:1986 卷标:(5) 页码:829-36]
109-94-4 = 922-65-6 反应条件:1.1 Reagents: Magnesium,Iodine Solvents: Tetrahydrofuran 标题:Novel Aspects Of The Chemistry Of Thioamides 作者:Naylor,Elizabeth Mary 参考文献:1987]
1219113-69-5 = 922-65-6 + 616-25-1 + 584-02-1 反应条件:1.1 Reagents: Methanol,Hydrogen Catalysts: Rhodium(1+),[(2,3,5,6-η)-Bicyclo[2.2.1]Hepta-2,5-Diene][(2S,2′s,5S,5′s)-1,1′-(1... Solvents: Methanol; 1.6 Atm,21 °C 标题:Stereoselectivity In The Rhodium-Catalyzed Reductions Of Non-Conjugated Dienes 作者:Nguyen,Bao; Brown,John M. 参考文献:Advanced Synthesis & Catalysis 日期:2009 卷标:351(9) 页码:1333-1343]
1826-67-1 = 922-65-6 反应条件:1.1 Solvents: Tetrahydrofuran; 0 °C; 1 H,Rt1.2 Reagents: Ammonium Chloride Solvents: Water; Rt 标题:Olefin-Migrative Cleavage Of Cyclopropane Rings Through The Nickel-Catalyzed Hydrocyanation Of Allenes And Alkenes 作者:Hori,Hiroto; Arai,Shigeru; Nishida,Atsushi 参考文献:Advanced Synthesis & Catalysis 日期:2017 卷标:359(7) 页码:1170-1176]
1826-67-1 = 922-65-6 反应条件:1.1 Solvents: Tetrahydrofuran; 0 °C; Overnight,0 °C1.2 Reagents: Ammonium Chloride Solvents: Water 标题:F- Nucleophilic-Addition-Induced Allylic Alkylation 作者:Tian,Panpan; Wang,Cheng-Qiang; Cai,Sai-Hu; Song,Shengjin; Ye,Lu; Et Al 参考文献:Journal Of The American Chemical Society 日期:2016 卷标:138(49) 页码:15869-15872]
专利号:US-5087703-A 优先权日:1988-01-28 标题 :Process for synthesis of FK-506 intermediates 发明人:VOLANTE RALPH P; ASKIN DAVID; SHINKAI ICHIRO; RYAN KENNETH M 权利人:MERCK & CO INC 摘要:A process is described for the synthesis of diastereomeric 2-methyl-4-hydroxy-5-protected-hydroxy-hept-6-en-prolinolamides, which are useful as intermediates in the synthesis of the C10-C18 chain of the macrolide structure for the immunosuppressant FK-506. These compounds are also useful as intermediates for preparing lactone ultraviolet radiation absorbers.
专利号:US-9879043-B1 优先权日:2013-06-06 标 题:Synthesis of non-natural cofactor analogs of S-adenosyl-L-methionine using methionine adenosyltransferase 发明人:THORSON JON; HUBER TYLER; ZHANG JIANJUN; Singh Shanteri 权利人:UNIV KENTUCKY RES FOUND 摘要:The present disclosure relates to the synthesis of non-natural analogs of S-adenosyl-L-methionine (SAM) and/or of Se-adenosyl-L-methionine (SeAM) by reacting a methionine analog and adenosine triphosphate (ATP) in the presence of at least one methionine adenosyltransferase (MAT), and to use thereof with downstream SAM and/or SeAM utilizing enzymes. The non-natural analogs of SAM and/or SeAM have the general formula: n nwhere X is S or Se, and R 1 is an alkyl group.
专利号:US-5637757-A 优先权日:1995-04-11 标 题 :One-pot synthesis of ring-brominated benzoate compounds 发明人:HILL JOHN E; FAVSTRITSKY NICOLAI A; MAMUZIC RASTKO I; BHATTACHARYA BHABATOSH 权利人:GREAT LAKES CHEMICAL CORP 摘要:A method of preparing tetrabromobenzoate compounds from tetrabromophthalic anhydride by reacting tetrabromophthalic anhydride with alcohol in the presence of a decarboxylation catalyst. The reaction may be carried out in an excess of alcohol, or with a near stoichiometric amount of alcohol by performing the reaction in an inert solvent.
专利号:US-2010298504-A1 优先权日:2007-09-19 标题 :Amphiphilic polymer and processes of forming the same 发明人:Janczewski Dominik; TOMCZAK NIKODEM; KHIN YIN WIN; HAN MINGYONG; VANCSO JULIUS 权利人:AGENCY SCIENCE TECH & RES 摘要:Disclosed are an amphiphilic polymer, its synthesis and uses thereof. The polymer has a hydrocarbon backbone with —COOH side groups. It further has first aliphatic moieties with a main chain of about 3 to about 20 carbon atoms and 0 to about 3 heteroatoms, and second aliphatic moieties that have a main chain of about 3 to about 80 carbon atoms and about 2 to about 40 heteroatoms. The second aliphatic moieties have a copolymerisable group. In the synthesis a maleic anhydride polymer of formula (I) where n is an integer from about 10 to about 10000 and R1 is H or methyl, is reacted with a monofunctional compound with an alkyl chain of about 3 to about 20 carbon atoms and 0 to about 2 heteroatoms, and with an at least bifunctional compound with an alkyl chain of about 3 to about 80 carbon atoms and 0 to about 40 heteroatoms. The functional group of the monofunctional compound and one functional group of the at least bifunctional compound can form a linkage with an anhydride. Another functional group of the at least bifunctional compound, which is not allowed to react with the maleic anhydride polymer, is copolymerisable.
专利号:US-2014114086-A1 优先权日:2012-10-22 标 题:Clinprost, Isocarbacyclin And Analogs Thereof And Methods Of Making The Same 发明人:CROATT MITCHELL 权利人:UNIV NORTH CAROLINA AT GREENSBORO 摘要:In one aspect, methods of synthesizing clinprost, isocarbacyclin and analogs thereof are described herein which, in some embodiments, permit an abbreviated synthetic pathway in comparison to one or more prior synthetic methods. By providing a compact synthetic scheme, methods described herein can reduce cost, waste and time of clinprost and isocarbacyclin synthesis while facilitating the development and investigation of analogs of these compounds.
专利号:US-9676676-B2 优先权日:2014-07-02 标题 :Selective olefin metathesis with cyclometalated ruthenium complexes 发明人:HARTUNG JR JOHN; QUIGLEY BRENDAN L; DORNAN PETER K; GRUBBS ROBERT H 权利人:CALIFORNIA INST OF TECHN 摘要:This invention relates generally to C—H activated ruthenium olefin metathesis catalyst compounds which are stereogenic at the ruthenium center, to their preparation, and the use of such catalysts in the metathesis of olefins and olefin compounds. In particular, the invention relates to the use of C—H activated ruthenium olefin metathesis catalyst compounds in Z-selective olefin metathesis reactions, enantio-selective olefin metathesis reactions, and enantio-Z-selective olefin metathesis reactions. The invention has utility in the fields of catalysis, organic synthesis, polymer chemistry, and industrial and fine chemicals chemistry.
摘要:Bubnov, Yu. N.; Kolomnikova, G. D., Science of Synthesis Knowledge Updates, (2012) 3, 317. 摘要:Matsumoto, K.; Katsuki, T.; Arends, I. W. C. E., Science of Synthesis: Stereoselective Synthesis, (2011) 1, 81. 摘要:Matsumoto, K.; Katsuki, T.; Arends, I. W. C. E., Science of Synthesis: Stereoselective Synthesis, (2011) 1, 76. 摘要:Szabó, K. J., Science of Synthesis: Multicomponent Reactions, (2013) 2, 351.