CAS: 2243-83-6; 2-Naphthoyl Chloride

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2351-36-2 879-18-5 66-99-9

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CAS号93-09-4 2-萘甲酸 | CAS号532-02-5 2-萘磺酸钠 | CAS号613-46-7 2-萘甲腈 | CAS号111876-50-7 4-naphthalen-2-... | CAS号105855-20-7 ethyl 1-(naphth... | CAS号107574-57-2 2-methyl-1-naph... | CAS号110876-52-3 2-甲基-1,2'-二萘酮 | CAS号39627-84-4 2-萘甲酰肼 | CAS号362669-46-3 ETHYL 8-(2-NAPH... | CAS号362669-52-1 8-(2-NAPHTHYL)-... | CAS号66832-24-4 2-[(trichlorome... | CAS号580-13-2 2-溴萘 | CAS号14625-56-0 2-naphthalen-2-...

2-萘甲腈置于五氯化磷,Potassium Carbonate体系中,化学反应生成2-萘甲酰氯
参考文献:Vieth,Justus Liebigs Annalen Der Chemie,1876,Vol. 180,P. 305
标题:Vieth,Justus Liebigs Annalen Der Chemie,1876,Vol. 180,P. 305

专利信息

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-6608196-B2
优先权日:2001-05-03
标题 :Process for solid supported synthesis of pyruvate-derived compounds
发明人：WANG BING; JANAGANI SATYANARAYANA; CALLAWAY WYETH B; SESSLER JONATHAN L
权利人:GALILEO PHARMACEUTICALS INC
摘要:Provided are processes for synthesizing structurally diverse pyruvate-derived compounds using a parallel approach on a solid phase support. Examples of such a solid phase support include resins which have also been used in solid phase peptide synthesis.

专利号:US-11981648-B2
优先权日:2019-06-13
标题:Method for the synthesis of 3-R-1,4,2-dioxazol-5-ones
发明人：HALL DAVID S; DAHN JEFFERY RAYMOND; HYNES TOREN
权利人:TESLA INC; PANASONIC HOLDINGS CORP
摘要:Provided are methods of preparing 3-R-1,4,2-dioxazol-5-one compounds using convenient and efficient methods. Also provided are 3-R-1,4,2-dioxazol-5-one compounds produced using the methods described.

专利号:US-2014046086-A1
优先权日:2012-08-10
标题:Process for the preparation of tafluprost and intermediates thereof
发明人：WEN WEN-HSIEN
权利人:SCINOPHARM CHANGSHU PHARMACEUTICALS LTD
摘要:The present invention provides efficient, economical and environmental friendly methods for synthesis of prostaglandin analogs including tafluprost and intermediates thereof. The invention involves a selective oxidation using in situ boronate ester protection and a unique crystallization method to remove the undesired isomers of fluorinated intermediates.

专利号:US-2014371316-A1
优先权日:2011-11-23
标 题:Derivatives of phenoxyisobutyric acid
发明人：LALEZARI IRAJ; FABRICANT JILL S
权利人:FABRICANT JILL S; LALEZARI IRAJ
摘要:The present invention provides a process for the synthesis of substituted phenoxymethylpropiomc acid and related compounds. The compounds are useful for inhibiting the formation of AGEs (Advanced Glycation End Products).

专利号:WO-2021081881-A1
优先权日:2019-10-31
标 题 :Functional carbohydrate molecule based on tdg molecular scaffold, and preparation method therefor
发明人：LI WEI; WANG HUAIYU
权利人:SHENZHEN INST ADV TECH
摘要:The present invention provides a carbohydrate compound, the structure of which is as represented by formula X, wherein R 1 and R 2 are independently selected from a substituted amido group, a substituted triazolyl group, and a substituted amino group; R 3 is selected from a sulfhydryl group, an azido group, an amino group, and a carboxyl group; A is formula aa or -C m H 2m R 3 , wherein X is selected from an oxygen atom; n is selected from 0, 1, 2, 3, 4, 5, 6, and 7; m is selected from 2, 3, 4, 5, 6, 7, 8, 9, and 10. In the present invention, a synthesis strategy of 'first side chain derivatization, then glycosylation coupling' is adopted, thereby achieving side chain derivatization modification of a TDG molecular scaffold and efficient synthesis of the compound . In the present invention , the use of the recognition and binding of a TDG glycoligand molecule to a target protein has a targeting function of identifying and binding to the target protein, and the TDG glycoligand molecule is used as a targeting molecule to construct a functional targeting molecule; the present invention has a wide application prospect in the fields such as tumor detection and tumor immunity.