CAS: 14320-37-7; Cyclopent-3-Enone

该化合物是一个多功能环球化合物,其特点是反应性的α,β-不饱和碳基结构.这五人环球酮是有机合成中有价值的中间体,特别是在建造复杂的分子框架方面.它的共聚系统能够参与迈克尔添加,迪埃尔斯-阿尔德反应和其他循环添加,使其对制药和精细化学应用有用.该化合物的紧张环环系统也有利于环形开关和功能化反应.分子重量为82.10克/摩尔,沸点约为120-122°C,它为实验室使用提供了可控处理特性.它的回动性和结构特征使得研究人员探索热循环和圆环系统成为首选.

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CAS号7129-41-1 6-噁双环[3.1.0]-3-己烯 | CAS号53859-89-5 hepta-1,6-dien-4-one | CAS号57260-93-2 4-methylsulfany... | CAS号875-20-7 tricyclo[5.2.1.... | CAS号27362-69-2 cyclopent-3-eny... | CAS号201230-82-2 carbon monoxide | CAS号542-92-7 环戊二烯 | CAS号185-94-4 housane | CAS号60410-16-4 (1R,4S)-4-羟基环戊-... | CAS号120-92-3 环戊酮 | CAS号14320-38-8 3-环戊烯-1-醇 | CAS号201230-82-2 carbon monoxide | CAS号106-99-0 丁二烯 | CAS号74017-10-0 6-oxabicyclo[3.... | CAS号60582-52-7 1-(4-cyclohepta... | CAS号60582-53-8 7-(4-cyclopenta...

合成工艺路线路线简述

    6-噁双环[3.1.0]-3-己烯置于[rh(1,5-Cyclooctadiene)(Ph2Pch2Ch2Pph2)][pf6]体系中,用 苯 用作溶剂,以30%的收率获得3-环戊烯-1-酮
    参考文献:区域和立体控制的α,β-不饱和羰基化合物的合成
    标题:区域和立体控制的α,β-不饱和羰基化合物的合成
    摘要:α,β-不饱和羰基化合物和丁烯化物可以通过铑(i)分别催化1,3-二烯单环氧化物和α-亚烷基-γ-丁内酯的异构化反应制备.前一种转化形式被正式认为是不对称酮的区域特异性醛醇缩合的等价物.
    Doi:10.1016/s0040-4039(00)98543-5

    海关参考信息

    专利信息


    专利号:US-11866398-B2
    优先权日:2018-05-15
    标 题:Total synthesis of prostaglandin J natural products by stereoretentive metathesis
    发明人:LI JIAMING; CHEN XU; AHMED TONIA S; STOLTZ BRIAN M; GRUBBS ROBERT H
    权利人:CALIFORNIA INST OF TECHN
    摘要:This invention relates generally to the synthesis of Δ12-Prostaglandin J product using stereoretentive ruthenium olefin metathesis catalysts supported by dithiolate ligands. Δ12-Prostaglandin J products were generated with excellent selectivity (>99% Z) and in moderate to high/good yields (47% to 80% yield; 58% to 80% yield).

    专利号:US-10995049-B2
    优先权日:2019-07-19
    标 题 :Total synthesis of prostaglandin J natural products and their intermediates
    发明人:LI JIAMING; XU CHEN; AHMED TONIA S; GRUBBS ROBERT H; STOLTZ BRIAN M
    权利人:CALIFORNIA INST OF TECHN
    摘要:The present disclosure is directed to methods of preparing prostaglandin J natural products by stereoretentive metatheses reactions and intermediates used in the synthesis of these natural products, including the use of intermediates of Formula (I-A), where R 1 is defined in the specification

    专利号:US-7910623-B2
    优先权日:2005-07-22
    标 题 :Synthesis of scabronines and analogues thereof
    发明人:DANISHEFSKY SAMUEL J; WATERS STEPHEN P
    权利人:SLOAN KETTERING INST CANCER
    摘要:A novel synthesis of scabronines, which are related to a broader class of angularly fused tricyclic diterpenoids known as cyathanes, is provided. Scabronine G, its methyl ester derivative, and other analogs have been shown to have neurotrophic activity. Therefore, these compounds are particularly useful in treating neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, Huntington's diseases, etc. The invention provides for the synthesis of scabronines as well as analogs thereof. Pharmaceutical compositions and method of using the inventive compounds are also provided.

    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-8426613-B2
    优先权日:2008-12-30
    标 题:Synthesis of substituted tetrahydroindenyl complexes
    发明人:VOSKOBOYNIKOV ALEXANDER Z; IZMER VYATCHESLAV V; KONONOVICH DMITRY S; RAZAVI ABBAS
    权利人:VOSKOBOYNIKOV ALEXANDER Z; IZMER VYATCHESLAV V; KONONOVICH DMITRY S; RAZAVI ABBAS; TOTAL PETROCHEMICALS RES FELUY
    摘要:This invention relates to the synthesis of substituted tetrahydroindenyls and the use of the synthesized complexes in the homo- and co-polymerization of ethylene and alpha-olefins.

    专利号:US-4762935-A
    优先权日:1986-10-06
    标题:Precursors and synthesis of methyl-9-oxo-11α,16-dihydroxy-16-vinyl-5-cis-13-trans-prostadienoates
    发明人:WISSNER ALLAN; GREEN KENNETH E; HAMANN PHILIP R; LEVIN JEREMY
    权利人:AMERICAN CYANAMID CO
    摘要:This disclosure describes novel compounds which are useful as precursors in the synthesis of 9-oxo-11α,16-dihydroxy-16-vinyl-5-cis-13-trans-prostadienoate esters which possess activity as hypotensive agents and/or as vasodilators.
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    合成参考文献


    摘要:Friesen, R. W., Science of Synthesis, (2001) 1, 181.
    摘要:Desmale, D., Science of Synthesis, (2005) 26, 359.
    摘要:Nakata, M., Science of Synthesis, (2007) 30, 414.
    摘要:Ogura, K., Science of Synthesis, (2007) 30, 462.
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