581-42-0 + 65051-83-4 + 496-11-7 + 573-98-8 + 569-41-5 + 527-53-7 + 575-41-7 = 119-64-2 + 27133-93-3 + 3296-50-2 + 4175-53-5 + 493-02-7 + 5325-97-3 反应条件:1.1 Reagents: Dodecane,Decane,Tridecane,Pentadecane,Hydrogen Catalysts: Ruthenium; 134.1 Bar; 3.25 H,157.6 Bar,Rt -> 305 °C 标题:An Improved Catalytic Pyrolysis Concept For Renewable Aromatics From Biomass Involving A Recycling Strategy For Co-Produced Polycyclic Aromatic Hydrocarbons 作者:Genuino,Homer C.; Muizebelt,Inouk; Heeres,Andre; Schenk,Niels J.; Winkelman,Jos G. M.; Et Al 参考文献:Green Chemistry 日期:2019 卷标:21(14) 页码:3802-3806]
= 119-64-2 + 530-91-6 反应条件:1.1 Reagents: Hydrogen Catalysts: Ruthenium Solvents: Methanol; Rt -> 170 °C; 60 Min,14 Mpa,170 °C 标题:Hydrogenation Of Hydroxy-Substituted Naphthalenes Using Ru And Ni Catalysts To Desired Decalols And Decalindiols 作者:Paterova,Iva; Et Al 参考文献:Reaction Kinetics 日期:2019 卷标:126(2) 页码:829-839]
= 119-64-2 + 89-72-5 + 2944-49-2 + 2082-61-3 + 1123-94-0 + 1197-34-8 反应条件:1.1 Reagents: Hydrogen Catalysts: Palladium; 1 H,350 °C; 4 H,350 °C 标题:Catalytic Hydrotreatment Of Pyrolytic Lignins From Different Sources To Biobased Chemicals: Identification Of Feed-Product Relations 作者:Figueiredo,M. B.; Deuss,P. J.; Venderbosch,R. H.; Heeres,H. J. 参考文献:Biomass And Bioenergy 日期:2020 卷标:134]
74543-59-2 = 119-64-2 [标题:Reaction Conditions 标题:The Intermediate Formation Of [4]Metacyclophane On Flash Vacuum Thermolysis 作者:Kostermans,Gerardus B. M.; Et Al 参考文献:Journal Of Organic Chemistry 日期:1988 卷标:53(19) 页码:4531-4]
613-80-9 = 119-64-2 反应条件:1.1 Reagents: Hydrogen Catalysts: Cobalt (Suppoted With N-Doped Carbon Material) Solvents: Hexane; 20 Bar,Rt; Rt -> 200 °C; 5 H,200 °C 标题:Selective Hydrogenolysis Of Lignin-Derived Aryl Ethers Over Co/c@n Catalysts 作者:Song,Qing-Lu; Et Al 参考文献:Renewable Energy 日期:2020 卷标:148 页码:729-738
萘烷置于环己烷,氢气,铂体系中,化学反应生成1,2,3,4-四氢萘 参考文献:Leroux,Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences,1910,Vol. 151,P. 384 标题:Leroux,Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences,1910,Vol. 151,P. 384
专利号:US-11926589-B2 优先权日:2019-07-09 标 题 :Process for the synthesis of non-racemic cyclohexenes 发明人:REISMAN SARAH; ROMBOLA MICHAEL; LADD CAROLYN L; MCLAUGHLIN MARTIN JOHN; ZUEND STEPHAN; GOETZ ROLAND 权利人:BASF CORP; CALIFORNIA INST OF TECHN 摘要:This invention relates to a process for the synthesis of a non-racemic cyclohexene compound of formula (I) by a Diels-Alder reaction of a compound of formula (II) with a compound of formula (III) wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and Y have the meanings as defined in the description in the presence of a catalyst comprising at least one m-valent metal cation M m+ wherein the metal M is selected from Scandium (Sc), Yttrium (Y), Lanthanum (La), Cerium (Ce), Praseodymium (Pr), Neodymium (Nd), Promethium (Pm), Samarium (Sm), Europium (Eu), Gadolinium 15 (Gd), Terbium (Tb), Dysprosium (Dy), Holmium (Ho), Erbium (Er), Thulium (Tm), Ytterbium (Yb), Lutetium (Lu), Gallium (Ga) and Indium (In), and m is an integer of 1, 2 or 3, and a chiral ligand of the formula (IV) wherein R 10a , R 10b , R 10c , R 10d , R 10a′ , R 10b′ , R 10c′ , R 10d′ , Z and Z′ have the meanings as defined in the description.
专利号:US-11161827-B2 优先权日:2019-04-05 标 题 :Catalytic systems for stereoselective synthesis of chiral amines by enantiodivergent radical C—H amination 发明人:Zhang xiao-xiang; Lang kai 权利人:TRUSTEES BOSTON COLLEGE; THE TRUSTEES OF BOSTON COLLEGE 摘要:In one aspect, the disclosure relates to a mode of asymmetric induction in radical processes based on sequential combination of enantiodifferentiative H-atom abstraction and stereoretentive radical substitution. Also disclosed is an asymmetric system for stereoselective synthesis of strained 5-membered cyclic sulfamides via radical 1,5-C—H amination of sulfamoyl azides. The disclosed metalloradical system can control the degree and sense of asymmetric induction in the catalytic radical C—H amination in a systematic manner. The disclosed system is applicable to a broad scope of substrates with different types of C(sp 3 )—H bonds and exhibits reactivity and selectivity, providing access to both enantiomers of useful 5-membered cyclic sulfamides in a highly enantioenriched form. Also disclosed are catalysts useful in these processes. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present disclosure.
专利号:US-2008032964-A1 优先权日:2006-04-10 标题:Process for the synthesis of azetidinone 发明人:KANSAL VINOD K; AHMAD SUHAIL; MARIAPPAN SHANMUGAVEL; TYAGI BHUPENDRA; PERLMAN NURIT; LE PAIH JACQUES; ZANOTTI-GEROSA ANTONIO 权利人:KANSAL VINOD K; AHMAD SUHAIL; MARIAPPAN SHANMUGAVEL; TYAGI BHUPENDRA; PERLMAN NURIT; LE PAIH JACQUES; ZANOTTI-GEROSA ANTONIO 摘要:Provided are intermediates useful for the synthesis of hydroxyl-alkyl substituted azetidinones, processes of their preparation, and processes for the synthesis of certain hydroxyl-alkyl substituted azetidinones. Also provided are processes for the synthesis of 1-(4-fluorophenyl)-3(R)-[3-(4-fluorophenyl)-3(S)-hydroxypropyl]-4(S)-(4-hydroxyphenyl)-2-azetidinone, or ezetimibe.
专利号:US-4399069-A 优先权日:1980-10-12 标题:Process for an enantioselective synthesis of optically active 14-oxo-E-homo-eburnane derivatives 发明人:SZANTAY CSABA; SZABO LAJOS; KALAUS GYORGY; SAPI JANOS; KREIDL JANOS; FARKAS NEE KIRJAK MARIA; NEMES ANDRAS; CIBULA LASZLO 权利人:RICHTER GEDEON VEGYESZET 摘要:The invention relates to a new enantioselective synthesis for the preparation of optically active 14-oxo-E-homo-eburnane derivatives of the formula (Ia) ##STR1## wherein R 1 is alkyl having from 1 to 4 carbon atom. In the synthesis optically active 6-alkoxycarbonylhexahydroindoloquinolizinium salts are employed as starting materials, which contain a center of chirality at the site of attachment of the carboxyl group. This center of chirality preserves the optical activity of the optically active tryptophan ester from which this compound has been prepared until a new center of chirality is formed in the molecule in a configuration corresponding to the desired end product. The carboxyl group, which is not needed in the end product and only serves to preserving the optical activity can then be eliminated. n Compounds of the formula (Ia) are known in the art and may be used in the synthesis of (+)-vincamine and (+)-apovincaminic acid ethylester.
专利号:US-8273790-B2 优先权日:2005-01-14 标 题:Exo-selective synthesis of himbacine analogs 发明人:THIRUVENGADAM TIRUVETTIPURAM K; SUDHAKAR ANANTHA; LIM NGIAP KIE; KWOK DAW-IONG; WU GEORGE G; WANG TAO; HUANG MINGSHENG; GREEN MICHAEL D 权利人:THIRUVENGADAM TIRUVETTIPURAM K; SUDHAKAR ANANTHA; LIM NGIAP KIE; KWOK DAW-IONG; WU GEORGE G; WANG TAO; HUANG MINGSHENG; GREEN MICHAEL D; SCHERING CORP 摘要:This application discloses a novel process for the synthesis of himbacine analogs, as well as the compounds produced thereby. The synthesis proceeds by alternative routes including the cyclic ketal amide route, the chiral carbamate amide route, and the chiral carbamate ester route. The compounds produced thereby are useful as thrombin receptor antagonists. The chemistry disclosed herein is exemplified in the following synthesis sequence:
专利号:US-2024092821-A1 优先权日:2020-03-31 标题:Synthesis of oligonucleotides and related compounds 发明人:ZHONG MINGHONG; JIN YI; GALA DINESH; PRHAVC MARIJA 权利人:JANSSEN BIOPHARMA INC 摘要:Methods of synthesizing oligonucleotides via new intermediates on a cleavable support having an azidomethyl moiety are disclosed. The method comprises multiple reaction cycles, each of which comprises sequential coupling a nucleoside or oligonucleotide subunit on a cleavable support having an azidomethyl moiety and a nucleoside phosphoramidite or an oligonucleotide phosphoramidite, capping, oxidation/thiolation and deblocking; followed by orthogonal cleavage of the azidomethyl support while keeping all other protecting groups intact. The method can be used in combination with a support moiety for either solid phase or liquid phase oligo synthesis. The soluble support facilitates homogeneous reactions and efficient separations by simple precipitation. The methods also provide novel intermediates useful in the synthesis of oligonucleotide conjugates.