专利检索_硫醛硫酮硫醌它们的氧化物专利检索_硫醛硫酮硫醌它们的氧化物专利检索查询

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序号	专利名	申请号	申请日	公开（公告）号	公开（公告）日	发明人
1	制备官能化烯烃的连续方法	CN99121308.4	1995-06-14	CN1258664A	2000-07-05	D·C·旦沃斯; J·I·艾默特; K·R·高达; W·D·戴安娜; J·E·斯塔纳特; W·B·艾克斯托姆; J·V·库素马诺; R·M·库洛斯; W·H·克罗斯; H·W·墨高
在CSTR或管式反应器中官能化烯烃,尤其聚合物烯烃的连续方法。优选由烯烃与一氧化碳和亲核捕集剂的连续反应生产酯类。充满液体的管式反应器按活塞流方式与静态混合机一起操作和CSTR在基本上没有空气的情况下在恒定的液面下进行操作。
2	BALANOIDS	PCT/US9402283	1994-03-02	WO9420062A3	1996-08-15	HALL STEVEN EDWARD; BALLAS LAWRENCE M; KULANTHAIVEL PALANIAPPAN; BOROS CHRISTIE; JIANG JACK B; JAGDMANN GUNNAR ERIK JR; LAI YEN-SHI; BIGGERS CHRISTOPHER K; HU HONG; HALLOCK YALI; HUGHES PHILIP F; DEFAUW JEAN MARIE; LYNCH MICHAEL PATRICK; LAMPE JOHN WILLIAM CROSSLEY; MENALDINO DAVID STEVEN; HEERDING JULIA MARIE; JANZEN WILLIAM P; HOLLINSHEAD SEAN PATRICK; NICHOLS JEFFREY BAILEY
A novel class of therapeutic compounds, denominated Balanoids, is disclosed. Balanoids have protein kinase C inhibitory activity and selectivity among the isoforms of protein kinase C. Balanoids are useful for treatment of diseases related to protein kinase C in animals, especially humans and is especially indicated for treatment of inflammatory diseases.
3	PEROXY ACID BLEACH PRECURSORS AND DETERGENT COMPOSITIONS CONTAINING THEM	PCT/US1991001700	1991-03-14	WO1991015474A1	1991-10-17	THE PROCTER & GAMBLE COMPANY; HARDY, Frederick, Edward
Novel highly water-soluble peroxyacid bleach precursor compounds are described of general formula (I), where R is methyl or ethyl, A is a C2-C6 alkylene, or phenylene group and Y is a sulphate, sulphonate quaternary ammonium or morpholinium group. Laundry bleaching and detergent compositions containing a source of alkaline hydrogen peroxide and one of said peroxyacid bleach precursor compounds provide enhanced bleaching and reduced colour and fabric damage relative to that provided by conventional precursors, at wash temperatures from 10 DEG C to 60 DEG C.
4	IMPROVED PROCESS FOR MAKING THIOBISCARBAMATES	EP83302110	1983-04-14	EP0092384B1	1986-12-30	FU, WALLACE YAM-TAK

5	BICYCLIC BENZENOID AMINOALKYLENE ETHERS AND THIOETHERS.	EP84902126	1984-04-27	EP0150192A4	1985-09-16	CAMPBELL HENRY FLUD; KUHLA DONALD ERNEST; STUDT WILLIAM LYON

6	PROCESS FOR PREPARING DL-CYSTEINE.	EP82901614	1982-05-26	EP0079966A4	1983-09-30	MITA RYUICHI; OHOKA MASAHARU; HIGUCHI CHOJIRO; KATOH TOSHIO; KAWASHIMA NOBUYUKI; YAMAGUCHI AKIHIRO; NAGAI SHOUSUKE; TAKANO TAKAO

7	LEPIDOPTERICIDAL ISOTHIOUREA COMPOUNDS.	EP80900649	1980-10-08	EP0027111A4	1982-04-08	FANCHER LLEWELLYN W; SCHER HERBERT B
Lepidoptericidal and herbicidal active compounds having the generic formula (FORMULA) wherein R, R1, R2 and R3 are as disclosed herein. In general, these compounds show enhanced lepidoptericidal activity and show reduced phytotoxic effect on crops to be protected from the lepidoptera.
8	3-(메틸티오)프로파날의 제조 방법(PROCESS FOR THE PREPARATION OF 3-(METHYLTHIO)PROPANAL)	KR1019970700180	1995-07-06	KR1019970704681A	1997-09-06	휴융씨.; 루에스트데니스에이.
본 발명은 3- (메틸티오)프로파날의 연속적인 제조 방법에 관한 것이다. 액체 반응 매질은 기체/액체 접촉 구역에서 기상 아크롤레인 공급 스트림과 접촉된다. 반응 매질은 3- (메틸티오)프로파탈, 메틸 메르캅탄 그리고 메틸 메르캅탄과 아크롤레인 사이의 반응용 촉매를 함유한다. 기상 아크렐레인 공급 스트림은 아크롤레인 증기와 비응축물 기체를 포함한다. 아크롤레인은 아크롤레인 공급 스트림에서 반응 매질로 전달되고 그 매질에서 메틸 메르캅탄과 반응해서 3- (메틸티오)프로파날을 함유하는 액체 반응 생성물을 제조한다. 비응축물 기체는 액체 반응 생성물에서 분리된다. 반응생성물 분획과 순환 분획으로 나누어지고, 순환 분획은 기체/액체 접촉 구역으로 재순환된다.
9	플루어로무틸린	KR1019900015650	1990-09-29	KR1019910007874A	1991-05-30	인골프마셔
내용 없음
10	2,2-비스-(2-퍼플루오로알킬에틸티오)-아세트알데히드의 제조방법	KR1019850008774	1985-11-23	KR1019860004196A	1986-06-18	브리지뜨베르때나; 애메깡뽕; 앙드레랑쯔
내용 없음
11	(±)-2-(톨릴술피닐)-시클로펜타데칸-1-온 및 그의 제법	KR1019960004716	1996-02-27	KR100179320B1	1999-05-15	박대규
본 발명은 신규 화합물인 하기 구조식(Ⅰ)의 (±)-2-(톨릴술피닐)-1-시클로펜타데칸-1-온 및 그의 제조 방법, 합성중간체로의 용도에 관한 것으로, 구조식(Ⅰ)의 신규화합물은 중추신경계에 작용하는 하기 구조식(Ⅱ)의 디엘-3-메칠-시클로펜타데칸-1-온의 제조시 합성중간체로 매우 유용하다.
12	(±)-2-(톨릴술피닐)-시클로펜타데칸-1-온 및 그의 제법	KR1019960004716	1996-02-27	KR1019970061862A	1997-09-12	박대규
본 발명은 신규 화합물인 하기 구조식(Ⅰ)의 ( + )-2-(톨릴술피닐)-시클로펜타데칸-1-온 및 그의 제조방법, 합성중간체로의 용도에 관한 것으로, 구조식(Ⅰ)의 신규 화합물은 중추신경계에 작용하는 하기 구조식(Ⅱ)의 디엘-3-메칠-시클로펜타데칸-1-온의 제조시 합성중간체로 매우 유용하다.
13	2,2-비스-(2-퍼플루오로알킬에틸티오)-아세트알데히드의 제조방법	KR1019850008774	1985-11-23	KR100040341B1	1991-03-12	브리지뜨베르때나; 애메깡뽕; 앙드레랑쯔

14	제초제 및 식물 생장 조절 특성을 갖는 아실시클로헥산디온과 그의 옥심 에테르의 제조방법	KR1019870003918	1987-04-23	KR1019870009990A	1987-11-30	한즈토블러
내용 없음
15	Helicenes exhibiting enhanced optical rotatory power	PCT/US9613553	1996-08-21	WO9708262A3	1997-04-24	KATZ THOMAS J; NUCKOLLS COLIN P
This invention provides an aggregate of a compound capable of forming helical structures such that the aggregate is capable of achieving a specific rotation of at least 100,000° for plane polarized light having a wavelength of 589 nm.
16	THIOSULPHINIC ACID DERIVATIVES, THEIR USE IN THE TREATMENT OF INFLAMMATORY DISEASES, AND DRUGS CONTAINING THEM	PCT/EP8800628	1988-07-12	WO8900422A3	1989-03-09	DORSCH WALTER; WAGNER HILDEBERT
Thiosulphinic acid derivatives, drugs containing these compounds, and their medicinal use. It has been discovered that thiosulphinic acid derivatives possess excellent anti-inflammatory properties. These compounds are particularly advantageous in the treatment of inflammatory processes induced by the platelet activation factor (PAF) in the bronchi.
17	USE OF MALONIC ACID DERIVATIVE COMPOUNDS FOR INCREASING CROP YIELD	PCT/US8700647	1987-03-30	WO8705897A3	1988-04-07	FRITZ CHARLES DAVID; COOKE ANSON RICHARD; MANNING DAVID TREADWAY; CAPPY JAMES JOSEPH; WHEELER THOMAS NEIL; MOORE BARBARA AUXIER
Increasing crop yield comprises applying a cpd. of formula (I), R1 and R2 are independently a substd. or unsubstd., carbocyclic or heterocyclic ring system, Y1 and Y2 are independently a substd. or unsubstd. heteroatom, Y3 and Y3 are independently hydrogen, or a substd. or unsubstd. heteroatom carbon atom, or a substd. or unsubstd. branched or straight chain contg. two or more carbon atoms or heteroatoms or (e.g.) halogen, alkylcarbonyl, formyl, alkylcarbonylalkyl, alkoxycarbonylalkyl, etc. Y5 and Y6 are independently oxygen or sulphur. -
18	HEXASUBSTITUTED CYCLOHEXANE COMPOUNDS	PCT/EP8700318	1987-06-19	WO8800940A3	1988-02-25	PRAEFCKE KLAUS; KOHNE BERND; DORSCH DIETER; RIEGER BERNHARD
Hexasubstituted cyclohexane compounds which are suitable as components of discotic liquid crystal phases.
19	SYNTHESIS OF ANTIULCER COMPOUNDS	PCT/EP8700172	1987-03-27	WO8705902A3	1987-11-19	REINER ALBERTO
To synthesize molecules with antiulcer action, specifically ranitidine, niperotidine and cimetidine, having the formula: (V) wherein R1 is hydrogen or together with R2 represents the rest of a cycloaliphatic or heterocyclic optionally substituted ring with 5 or 6 carbon atoms, R2 represents H, alkyl, alkyl substituted with a simple or substituted aromatic ring or with a single or substituted heterocyclic ring, Ar represents a simple or substituted phenyl group, a simple or substituted heterocyclic aromatic group, N=1, 2, 3, 4, 5 or 6 and X represents CH-NO2, S, N-C 3BOND N, the compound (II) is prepared through the following process sequence: (II) +TR wherein Z=H, NO2, halogen and R3=-(CH2)n Ar, -(CH2)n -SH, -(CH2)n-S-S-(CH2)n, -(CH2)n-S-CH2Ar Y being halogen. The urea of formula (II) is converted in a first stage into the corresponding carbodiimide (VI) by reaction with triphenylphosphine and bromine in the presence of a strong base and in a second stage is obtained the desired compound by reaction with nitromethane or with a saline derivative of cynamide.
20	PROCESS FOR THE PRODUCTION OF ALKYLENE OR CYCLICALLY LINKED COMPOUNDS	PCT/EP8700527	1987-09-16	WO8802357A3	1988-06-16	POETSCH EIKE; REIFFENRATH VOLKER
Compounds having formula (I): R<1>-(A)k-(Z<1>-A<1>)m-Z-(E)n-(Q)o-(Z<2>-A<2>)p-R<2>, can be easily produced in high yields from organic zinc compounds having formula (II): R<1>-(A)k-(Z<1>-A<1>)m-Z-ZnY and compounds having formula (III): X-(E)n-(Q)o-(Z<2>-A<2>)p-R<2>, in which A, A<1>, A<2>, E, R<1>, R<2>, Z, Z<1>, Z<2>, Q, k, m, n, o and p have the given meaning.

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