CAS: 1678-92-8; Propylcyclohexane

相似化合物

54105-66-7 1795-16-0 6006-33-3

上下游产品

CAS号645-56-7 4-丙基苯酚 | CAS号2114-42-3 烯丙基环己烷 | CAS号97-53-0 丁香酚 | CAS号2785-87-7 2-甲氧基-4-丙基苯酚 | CAS号6627-88-9 4-烯丙基-2,6-二甲氧基苯酚 | CAS号2503-46-0 4-羟基-3-甲氧基苯丙酮 | CAS号103-65-1 正丙苯溶液标准物质 | CAS号635-46-1 1,2,3,4-四氢喹啉 | CAS号300-57-2 烯丙基苯 | CAS号2539-75-5 1-propyl-Cyclohexene | CAS号7094-27-1 1,1,4-三甲基环己烷 | CAS号2234-75-5 1,2,4-三甲基环己烷 | CAS号1795-27-3 (1Alpha,3Alpha,... | CAS号3073-66-3 1,1,3-三甲基环己烷 | CAS号7094-26-0 1,1,2-三甲基环己烷 | CAS号1678-97-3 1,2,3-三甲基环己烷 | CAS号1839-63-0 1,3,5-三甲基环己烷 | CAS号74-98-6 丙烷 | CAS号187737-37-7 propene | CAS号34557-54-5 methane

📜茴香烯置于镍,溶剂黄146,铂体系中,50.0 °C,12.75 Mpa 条件下,反应生成正丙基环己烷
参考文献:The Isomeric 4-N-Propylcyclohexanols1
标题:The Isomeric 4-N-Propylcyclohexanols1
摘要:
Doi:10.1021/jo01182A004

专利信息

专利号:WO-9517903-A1
优先权日:1993-12-28
标 题:Modular design and synthesis of oxazolone-derived molecules
发明人：HOGAN JOSEPH C JR; CASEBIER DAVID; FURTH PAUL; TU CHENG
权利人:ARQULE PARTNERS L P; HOGAN JOSEPH C JR; CASEBIER DAVID; FURTH PAUL; TU CHENG
摘要:The design and synthesis of novel oxazolone-derived molecular modules and the use of the modules in the construction of new molecules and fabricated materials is disclosed. The new molecules and fabricated materials are molecular recognition agents useful in the design and synthesis of drugs, and have applications in separations and materials science.

专利号:US-2003162992-A1
优先权日:2001-12-14
标 题 :Preparation of intermediates useful in the synthesis of antiviral nucleosides
发明人：WATANABE KYOICHI A; DU JINFA
摘要:The present invention is an efficient process for the manufacture of α-acyloxyacetaldehyde, a key intermediate in the synthesis of 1,3-oxathiolane and 1,3-dioxolane nucleosides.

专利号:US-4190579-A
优先权日:1977-12-29
标题:Synthesis of beta-lactams from azetidine carboxylic acid esters
发明人：LIPSHUTZ BRUCE H; WASSERMAN HARRY H; WU JAMES S
权利人:RESEARCH CORP
摘要:Azetidine carboxylic acid esters are converted into enol silyl ethers which, as enamino ketene acetals, undergo ready oxidative cleavage of the ethylenically unsaturated double bond, e.g. by dye-sensitized photo-oxygenation, to form beta-lactams. The beta-lactams and substitution products thereof are useful intermediates in the synthesis of biologically active lactams.

专利号:US-9676726-B2
优先权日:2013-12-23
标题:Process for the regioselective synthesis of pyrazoles
发明人：MEAZZA GIOVANNI; SILLANI LAURA; MEREGHETTI PIERANGELO; FORGIA DANIELE
权利人:ISAGRO SPA
摘要:A process is described for the synthesis of pyrazoles having general formula (I) n nwhich comprises the steps of mixing a compound having general formula (II)n n nand a 1,2-disubstituted hydrazine having general formula (III)n n nto form a reaction intermediate having general formula (IV)n n nand the reaction mixture obtained in step i), in an acid environment, cyclizes to form a pyrazole having general formula (I), according to reaction scheme 1

专利号:US-10829792-B2
优先权日:2017-03-21
标 题 :Biocatalytic synthesis of strained carbocycles
发明人：CHEN KAI; HUANG XIONGYI; KAN S B JENNIFER
权利人:CALIFORNIA INST OF TECHN
摘要:Provided herein are methods for producing products containing strained carbocycles, such as cyclopropene moieties and/or bicyclobutane moieties. The methods include combining an alkyne and a carbene precursor in the presence of a heme protein, e.g., a cytochrome P450, under conditions sufficient to form the strained carbocycle. Reaction mixtures for producing strained carbocycles are also described, as well as whole-cell catalysts comprising heme proteins and variants thereof for forming cyclopropenes, bicyclobutanes, and related products.

专利号:US-11897914-B2
优先权日:2021-11-29
标题 :Synthesis of 2′ protected nucleosides
发明人：POON WING C; ZOU RUIMING; LAU ALDRICH N K; YU DAVID; Du Gengyu; YAO YUN-CHIAO; ZHAO GANG
权利人:HONGENE BIOTECH CORP
摘要:Embodiments of the present application relate to the preparation of 2′-O-protected nucleoside phosphoramidites and conjugation of the 2′-O-protected nucleoside to a solid support. More specifically, the present application relates to nucleosides having a hydroxy protecting group at the 2′ position that reduces migration to the 3′ position during RNA (e.g., mRNA) synthesis and can be readily removed under mild conditions without the use of toxic metal-containing reagents. Methods of using the nucleosides described herein in RNA synthesis are also disclosed.