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公开(公告)号:US09708351B2
公开(公告)日:2017-07-18
申请号:US15143669
申请日:2016-05-02
IPC分类号: C07C17/093 , C07C29/42 , C07F7/22 , C07C1/32 , C07C45/00 , C07D333/08 , C07D213/16 , C07D239/26 , C07C253/30 , C07C41/01 , C07C41/16 , C07C41/30 , C07C67/333
CPC分类号: C07F7/2208 , C07C1/325 , C07C17/093 , C07C29/42 , C07C41/01 , C07C41/16 , C07C41/30 , C07C45/00 , C07C45/67 , C07C67/333 , C07C253/30 , C07C2603/10 , C07C2603/24 , C07D213/16 , C07D239/26 , C07D333/08 , C07C255/50 , C07C33/28 , C07C43/1787 , C07C43/166 , C07C43/225 , C07C43/20 , C07C69/618 , C07C15/24 , C07C15/28 , C07C49/784
摘要: Disclosed are methods for rerouting radical cascade cyclizations by using alkenes as alkyne equivalents. The reaction sequence is initiated by a novel 1,2 stannyl shift which achieves chemo- and regioselectivity in the process. The radical “hopping” leads to the formation of the radical center necessary for the sequence of selective cyclizations and fragmentations to follow. In the last step of the cascade, the elimination of a rationally designed radical leaving group via β-C—C bond scission aromatizes the product without the need for external oxidant. The Bu3Sn moiety, which is installed during the reaction sequence, allows further functionalization of the product via facile reactions with electrophiles as well as Stille and Suzuki cross-coupling reactions. This selective radical transformation opens a new approach for the controlled transformation of enynes into extended polycyclic structures of tunable dimensions.
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公开(公告)号:US08501715B2
公开(公告)日:2013-08-06
申请号:US13085542
申请日:2011-04-13
申请人: Dror Harats , Jacob George , Gideon Halperin , Itzhak Mendel , Niva Yacov , Eti Kovalevski-Ishai
发明人: Dror Harats , Jacob George , Gideon Halperin , Itzhak Mendel , Niva Yacov , Eti Kovalevski-Ishai
CPC分类号: C07F9/106 , A61K31/075 , A61K31/08 , A61K31/11 , A61K31/19 , A61K31/20 , A61K31/215 , A61K31/225 , A61K31/24 , A61K31/685 , C07C43/13 , C07C43/1785 , C07C43/1787 , C07F9/10 , Y02A50/411 , Y02A50/414
摘要: Novel synthetic oxidized lipids and methods utilizing oxidized lipids for treating and preventing an inflammation associated with an endogenous oxidized lipid are provided.
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公开(公告)号:US07902176B2
公开(公告)日:2011-03-08
申请号:US10567543
申请日:2004-05-27
申请人: Dror Harats , Jacob George , Gideon Halperin , Niva Yacov , Eti Kovalevski-Ishai
发明人: Dror Harats , Jacob George , Gideon Halperin , Niva Yacov , Eti Kovalevski-Ishai
CPC分类号: C07F9/106 , A61K31/075 , A61K31/08 , A61K31/11 , A61K31/19 , A61K31/20 , A61K31/215 , A61K31/225 , A61K31/24 , A61K31/685 , C07C43/13 , C07C43/1785 , C07C43/1787 , C07F9/10 , Y02A50/411 , Y02A50/414
摘要: Novel synthetic oxidized lipids and methods utilizing oxidized lipids for treating and preventing an inflammation associated with an endogenous oxidized lipid are provided.
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公开(公告)号:US20050288525A1
公开(公告)日:2005-12-29
申请号:US10504831
申请日:2003-03-03
申请人: James Leighton , Xiaolun Wang , James Kinnaird
发明人: James Leighton , Xiaolun Wang , James Kinnaird
IPC分类号: C07C29/38 , C07C33/14 , C07C33/20 , C07C41/30 , C07C41/56 , C07C43/178 , C07C43/23 , C07C241/02 , C07C241/04 , C07C243/28 , C07C243/32 , C07F7/02 , C07F7/04 , C07F7/08 , C07F7/10 , C07F7/12 , C07F7/18
CPC分类号: C07C403/08 , C07B2200/07 , C07C29/38 , C07C41/30 , C07C43/1787 , C07C43/23 , C07C241/04 , C07C2601/14 , C07F7/045 , C07F7/12 , C07F7/122 , C07F7/1804 , C07F7/1876 , C07F7/188 , C07C243/28 , C07C33/48 , C07C33/03 , C07C33/14 , C07C33/26 , C07C33/30
摘要: A new class of reagents and method of use of the reagents in the reaction of the reagents with electrophilic compounds. The invention in one embodiment is directed to a method for the formation of an alcohol of the formula (I). The method includes reacting reagent of the formula (II) with an aldehyde of the formula R10CHO to form the alcohol. X3 is one of O and C(R4)(R5). Each of X1 and X2 is independently O or N—R. Each of Ca and Cb is independently an achiral center, an (S) chiral center or an (R) chiral center. Ra and Rb are (i) each independently C1-10 alkyl, C6-10 aryl or C3-9 heteroaryl, or (ii) taken together to form a C3-C4 alkylene chain which together with Ca and Cb forms a 5-membered or 6-membered aliphatic ring. Rc and Rd are each independently hydrogen, C1-10 alkyl, C6-10 aryl or C3-9 heteroaryl. R is C1-10 alkyl, C6-10 aryl or C3-9 heteroaryl. Each of R1, R2, R3, R4, R5 is independently hydrogen, C1-C10 alkyl, C6-10 aryl, C3-9 heteroaryl, C1-10 alkoxy, C6-10 aryloxy, C1-10 dialkylamino, C1-10 alkyl-C6-10 arylamino, C1-10 diarylamino, or halogen. R6 is halogen, hydrogen, C1-10 alkyl, C6-10 aryl, C3-9 heteroaryl, C1-10 alkoxy, C6-10 aryloxy, C1-10 alkyl-C6-10 arylamino, C1-10 diarylamino, OSO2CF3 or SR. R10 may be C1-10 alkyl, C6-10 aryl, or C3-9 heteroaryl.
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公开(公告)号:US20030225035A1
公开(公告)日:2003-12-04
申请号:US10445347
申请日:2003-05-27
发明人: Dror Harats , Jacob George , Gideon Halperin
IPC分类号: A61K031/685 , C07F009/02
CPC分类号: C07F9/106 , A61K31/075 , A61K31/08 , A61K31/11 , A61K31/19 , A61K31/20 , A61K31/215 , A61K31/225 , A61K31/24 , A61K31/685 , C07C43/13 , C07C43/1785 , C07C43/1787 , C07F9/10 , Y02A50/411 , Y02A50/414
摘要: Novel synthetic forms of etherified oxidized phospholipids and methods of utilizing same for preventing and treating atherosclerosis and other related disorders, as well as inflammatory disorders, immune mediated diseases, autoimmune diseases and proliferative disorders, are provided. In addition, methods of synthesizing etherified and esterified oxidized phospholipids and of using same for preventing and treating atherosclerosis and other related disorders are also provided.
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公开(公告)号:US06326520B1
公开(公告)日:2001-12-04
申请号:US09377688
申请日:1999-08-20
申请人: Akihiro Ishii , Koichi Mikami
发明人: Akihiro Ishii , Koichi Mikami
IPC分类号: C07C49213
CPC分类号: C07F7/1892 , B01J31/223 , B01J2231/341 , B01J2531/0266 , B01J2531/46 , C07C43/1787 , C07C45/30 , C07C49/82
摘要: The invention relates to a method for producing a novel optically active compound represented by the general formula [IV]. This method includes the step of reacting a vinyl ether with a halogenated acetaldehyde in the presence of an optically active binaphthol-titanium complex. With this, the novel optically active compound can be produced very easily. Furthermore, the novel optically active compound can easily be oxidized to a novel optically active &agr;,&bgr;-dihydrexyketone represented by the general formula [V]. These novel optically active compounds can each be used as useful intermediates. where R is a lower alkyl group or —Si(R3)3, where R3 is a lower alkyl group and three of R3 may be the same or different groups, R1 is a lower alkyl group or a substituted or unsubstituted phenyl group, R2 is hydrogen atom or a lower alkyl group or a substituted or unsubstituted phenyl group, or R1 and R2 are combined to form an alkylene group, and X is hydrogen, fluorine, chlorine or bromine with a proviso that three of said X may be the same or different atoms, but are not hydrogen at the same time.
摘要翻译: 本发明涉及一种由通式[Ⅳ]表示的新的光学活性化合物的制备方法。 该方法包括在光学活性联萘酚钛络合物存在下使乙烯基醚与卤代乙醛反应的步骤。 由此,可以非常容易地制造新颖的光学活性化合物。 此外,新的光学活性化合物可以容易地被氧化成由通式[V]表示的新的光学活性α,β-二羟基酮。 这些新的光学活性化合物各自可用作有用的中间体。其中R是低级烷基或-Si(R3)3,其中R3是低级烷基,R3中的三个可以是相同或不同的基团,R1是 低级烷基或取代或未取代的苯基,R 2为氢原子或低级烷基或取代或未取代的苯基,或R 1和R 2结合形成亚烷基,X为氢,氟,氯或溴 条件是所述X中的三个可以是相同或不同的原子,但不是同时是氢。
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公开(公告)号:US06306988B1
公开(公告)日:2001-10-23
申请号:US09491800
申请日:2000-01-26
IPC分类号: C08F426
CPC分类号: C07C269/06 , C07C41/30 , C07C67/475 , C07C69/78 , C07C69/007 , C07C69/16 , C07C43/166 , C07C43/1787
摘要: A method for the cross-metathesis of terminal olefins is disclosed. The method describes making disubstituted internal olefin products by contacting a first terminal olefin with another first terminal olefin to form a dimer and then contacting the dimer with a second terminal olefin in the presence of a catalyst having the formula where M may be Os or Ru, R and R1 may be the same or different and may be hydrogen or a substitutent group selected from C1-C20 alkyl, C2-C20 alkenyl,C2-C20 alkynyl, aryl, C1-C20 carboxylate, C1-C20 alkoxy, C2-C20 alkenyloxy, C2-C20 alkynyloxy, aryloxy, C2-C20 alkoxycarbonyl, C1-C20 alkylthio, C1-C20 alkylsulfonyl, and C1-C20 alkylsulfinyl. X and X1 may be the same or different and may be any anionic ligand. L and L1 may be the same or different and may be any neutral electron donor.
摘要翻译: 公开了一种用于末端烯烃交叉复分解的方法。 该方法描述了通过使第一末端烯烃与另一个第一末端烯烃接触以形成二聚体制备二取代的内烯烃产物,然后在具有式I的催化剂存在下使二聚体与第二末端烯烃接触,M可以是Os或Ru,R 并且R 1可以相同或不同,并且可以是氢或选自C 1 -C 20烷基,C 2 -C 20烯基,C 2 -C 20炔基,芳基,C 1 -C 20羧酸酯,C 1 -C 20烷氧基,C 2 -C 20链烯氧基, C 2 -C 20炔氧基,芳氧基,C 2 -C 20烷氧基羰基,C 1 -C 20烷硫基,C 1 -C 20烷基磺酰基和C 1 -C 20烷基亚磺酰基。 X和X 1可以相同或不同,并且可以是任何阴离子配体。 L和L1可以相同或不同,并且可以是任何中性电子给体。
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公开(公告)号:US5385996A
公开(公告)日:1995-01-31
申请号:US72687
申请日:1993-06-07
申请人: Ezio Rizzardo , Gordon F. Meijs , San H. Thang
发明人: Ezio Rizzardo , Gordon F. Meijs , San H. Thang
IPC分类号: C07C43/176 , C07C43/178 , C07C43/215 , C07C323/25 , C07F7/18 , C07F9/40 , C08F2/38 , C08F246/00
CPC分类号: C07C323/60 , C07C255/00 , C07C321/00 , C07C323/00 , C07C323/25 , C07C43/176 , C07C43/1787 , C07C43/215 , C07F7/1852 , C07F9/4015 , C08F246/00
摘要: A process for the production of polymers by free radical polymerization, characterized in that there is added to the polymerization system one or more compounds of the general formula (A). ##STR1## where R.sup.1 is hydrogen or a group capable activating the vinylic carbon towards free radical addition;Y is OR.sup.2 or CH.sub.2 X(R.sup.2).sub.nwhere R.sup.2 is an optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, or optionally substituted saturated, unsaturated or aromatic, aromatic carbocyclic or heterocyclic ring;X is an element other than carbon selected from Groups IV, V, VI or VII of the Periodic Table or a group consisting of an element selected from Groups IV, V, or VI to which is attached one or more oxygen atoms; andn is a number from 0 to 3, such that the valency of the group X is satisfied and, when n is greater than 1, the groups represented by R.sup.2 may be identical or different.
摘要翻译: 通过自由基聚合制备聚合物的方法,其特征在于向聚合体系中加入一种或多种通式(A)的化合物。 (A)其中R1是氢或能够将乙烯基碳活化成自由基添加的基团; Y是OR2或CH2X(R2)n,其中R2是任选取代的烷基,任选取代的烯基,任选取代的炔基或任选取代的饱和,不饱和或芳族芳族碳环或杂环; X是除了选自元素周期表第Ⅳ,Ⅴ,Ⅵ或Ⅶ族的碳以外的元素,或由选自附有一个或多个氧原子的第Ⅳ,Ⅴ或Ⅵ族元素组成的组元素; 并且n为0至3的数,使得满足基团X的化合价,并且当n大于1时,由R 2表示的基团可以相同或不同。
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公开(公告)号:US4129599A
公开(公告)日:1978-12-12
申请号:US809237
申请日:1977-06-23
申请人: Sina Escher , Grant E. Dubois
发明人: Sina Escher , Grant E. Dubois
IPC分类号: C07C29/147 , C07C43/178 , C07C45/29 , C07C45/41 , C07C45/66 , C07C47/20 , C07C47/24 , C07C49/255 , C07C49/61
CPC分类号: C07C29/147 , C07C43/1787 , C07C45/29 , C07C45/292 , C07C45/41 , C07C45/66 , C07C47/20 , C07C47/24 , C07C49/255 , C12C11/02 , C07C2101/10
摘要: Method is provided for cyclization of polyunsaturated substituted acylic or monocarbocyclic initiator group containing compound having an endocyclic double bond with a chalcogen atom in the allylic position of the initiator group and having at least two sites of unconjugated aliphatic unsaturation in the side chain substituent on the ring. The polyunsaturated compound is cyclized in the presence of a strong acid in a protic solvent which is inert to the acid, preferably a hydroxylic solvent. Mild temperatures and varying times are employed. The products are useful primarily as intermediates for naturally occurring and synthetic steroids. By appropriate substitution of the side chain, the steroidial products are provided with the substituent at C-11, which upon cyclization results in the alpha-configuration. By resolution of the intermediates prior to cyclization, optically active steroids can be obtained.
摘要翻译: 提供了用于在引发剂基团的烯丙基位置环化多不饱和取代的含酰基或单环引发剂基的含有内环双键的化合物与硫属化合物原子并且在环上的侧链取代基中具有至少两个未偶联的脂族不饱和位点 。 多不饱和化合物在强酸存在下,在对酸,优选羟基溶剂惰性的质子溶剂中环化。 采用温和的温度和变化的时间。 该产品主要用作天然存在和合成类固醇的中间体。 通过侧链的适当取代,在C-11处提供了具有取代基的类固醇产物,其在环化时产生α构型。 通过在环化前分解中间体,可以获得光学活性类固醇。
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公开(公告)号:US20180065908A1
公开(公告)日:2018-03-08
申请号:US15811277
申请日:2017-11-13
申请人: Xiamen University
发明人: Haiping XIA , Qingde ZHUO , Jianfeng LIN , Xiaoxi ZHOU , Zhixin CHEN , Yifan SHAO , Hong ZHANG , Xumin HE
IPC分类号: C07C33/04 , C07C43/178
CPC分类号: C07C33/04 , C07C29/00 , C07C41/18 , C07C43/178 , C07C43/1781 , C07C43/1787 , C07C67/317 , C07C69/606 , C07C69/732 , C07C205/04 , C07C205/56 , C07C253/30 , C07C255/15 , C07C303/40 , C07C311/17 , C07C2601/02 , C07C2601/08 , C07C2601/14 , C07C2603/50 , C07D307/40 , C07D333/16 , C07D333/24 , C07F13/00 , C07F15/0033 , C07F15/0046 , C07F15/0073 , H01L31/00
摘要: The present invention relates to fields of organic chemistry and organometallic chemistry. The present invention discloses a chain multiyne compound, a preparation method thereof and an application in synthesizing a fused-ring metallacyclic compound. A structure of the chain multiyne compound in the present invention is shown as Formula I below. The present invention also provides a preparation method of the chain multiyne compound and an application thereof in a synthesis of a fused-ring metallacyclic compound. The chain multiyne compound disclosed in the present invention has multiple functional groups and the structure of the chain multiyne compound is adjustable. The chain multiyne compound can also be used to synthesize the fused-ring metallacyclic compound efficiently. The preparation method of the chain multiyne compound disclosed in the present invention is simple, which can be used to prepare the chain multiyne compound rapidly and efficiently.
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