GB1257111A - - Google Patents
Info
- Publication number
- GB1257111A GB1257111A GB1257111DA GB1257111A GB 1257111 A GB1257111 A GB 1257111A GB 1257111D A GB1257111D A GB 1257111DA GB 1257111 A GB1257111 A GB 1257111A
- Authority
- GB
- United Kingdom
- Prior art keywords
- give
- amino
- phenylaziridine
- aziridine
- imino
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- TXUGGXZUGGCMBM-UHFFFAOYSA-N 2h-azirin-3-amine Chemical compound NC1=NC1 TXUGGXZUGGCMBM-UHFFFAOYSA-N 0.000 abstract 5
- 150000007857 hydrazones Chemical class 0.000 abstract 4
- 150000001299 aldehydes Chemical class 0.000 abstract 3
- 125000003700 epoxy group Chemical group 0.000 abstract 3
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical compound COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 abstract 2
- -1 2-nitrophenyl Chemical group 0.000 abstract 2
- KNKDTKBMUZNQOZ-UHFFFAOYSA-N 2-phenylaziridin-1-amine Chemical compound NN1CC1C1=CC=CC=C1 KNKDTKBMUZNQOZ-UHFFFAOYSA-N 0.000 abstract 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 2
- 235000018734 Sambucus australis Nutrition 0.000 abstract 2
- 244000180577 Sambucus australis Species 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- RLFFLEZFARXFQF-UHFFFAOYSA-N aziridin-1-amine Chemical class NN1CC1 RLFFLEZFARXFQF-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 150000001923 cyclic compounds Chemical class 0.000 abstract 2
- 238000004817 gas chromatography Methods 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- KZPROGSHDIYCJJ-UHFFFAOYSA-N (2-methylsulfonyloxy-2-phenylethyl) methanesulfonate Chemical compound CS(=O)(=O)OCC(OS(C)(=O)=O)C1=CC=CC=C1 KZPROGSHDIYCJJ-UHFFFAOYSA-N 0.000 abstract 1
- OAVZVNDSDPGHBL-UHFFFAOYSA-N 1-(6-oxabicyclo[3.1.0]hexan-1-yl)ethanone Chemical compound C1CCC2OC21C(=O)C OAVZVNDSDPGHBL-UHFFFAOYSA-N 0.000 abstract 1
- LSFWDFKKMLUPNK-UHFFFAOYSA-N 1-(7-oxabicyclo[4.1.0]hept-3-en-6-yl)propan-1-one Chemical compound C1C=CCC2OC21C(=O)CC LSFWDFKKMLUPNK-UHFFFAOYSA-N 0.000 abstract 1
- SLNPSLWTEUJUGY-UHFFFAOYSA-N 1-(cyclopenten-1-yl)ethanone Chemical compound CC(=O)C1=CCCC1 SLNPSLWTEUJUGY-UHFFFAOYSA-N 0.000 abstract 1
- XBLNZHWIDWYLEY-UHFFFAOYSA-N 2-(5-ethynyl-3,6,6-trimethyl-1,2,3,4,5,6a-hexahydropentalen-3a-yl)acetaldehyde Chemical compound C(=O)CC12CC(C(C2CCC1C)(C)C)C#C XBLNZHWIDWYLEY-UHFFFAOYSA-N 0.000 abstract 1
- WPHUUIODWRNJLO-UHFFFAOYSA-N 2-nitrobenzenesulfonyl chloride Chemical compound [O-][N+](=O)C1=CC=CC=C1S(Cl)(=O)=O WPHUUIODWRNJLO-UHFFFAOYSA-N 0.000 abstract 1
- MITSHSPZPXEKGA-UHFFFAOYSA-N 2H-azirin-3-amine hex-5-ynal Chemical compound C(CCCC#C)=O.N=C1NC1 MITSHSPZPXEKGA-UHFFFAOYSA-N 0.000 abstract 1
- WTEVFHFQWNTPQP-UHFFFAOYSA-N 6-methyl-7-oxabicyclo[4.1.0]heptan-5-one Chemical compound C1CCC(=O)C2(C)C1O2 WTEVFHFQWNTPQP-UHFFFAOYSA-N 0.000 abstract 1
- NIHGVELXFBDHAE-UHFFFAOYSA-N 6-oxabicyclo[3.1.0]hexane-1-carbaldehyde Chemical compound C1CCC2OC21C=O NIHGVELXFBDHAE-UHFFFAOYSA-N 0.000 abstract 1
- FOWXHCKXNRLLOZ-UHFFFAOYSA-N 7-azabicyclo[4.1.0]heptan-7-amine Chemical compound C1CCCC2N(N)C21 FOWXHCKXNRLLOZ-UHFFFAOYSA-N 0.000 abstract 1
- DINLIZUFVHTMDX-UHFFFAOYSA-N 7-azabicyclo[4.1.0]heptane Chemical compound C1CCCC2NC21 DINLIZUFVHTMDX-UHFFFAOYSA-N 0.000 abstract 1
- QKOHEJBTNOEACF-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-5-one Chemical compound O=C1CCCC2OC12 QKOHEJBTNOEACF-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- 239000012359 Methanesulfonyl chloride Substances 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001728 carbonyl compounds Chemical class 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- RALDHUZFXJKFQB-UHFFFAOYSA-N cyclopentene-1-carbaldehyde Chemical compound O=CC1=CCCC1 RALDHUZFXJKFQB-UHFFFAOYSA-N 0.000 abstract 1
- RHUDTGURSKUCFK-UHFFFAOYSA-N dec-4-ynal Chemical compound C(CCC#CCCCCC)=O RHUDTGURSKUCFK-UHFFFAOYSA-N 0.000 abstract 1
- 150000002009 diols Chemical class 0.000 abstract 1
- IHQPHCUJVGKQHD-UHFFFAOYSA-N dodec-4-ynal Chemical compound C(CCC#CCCCCCCC)=O IHQPHCUJVGKQHD-UHFFFAOYSA-N 0.000 abstract 1
- VGEWEGHHYWGXGG-UHFFFAOYSA-N ethyl n-hydroxycarbamate Chemical compound CCOC(=O)NO VGEWEGHHYWGXGG-UHFFFAOYSA-N 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 239000012634 fragment Substances 0.000 abstract 1
- 238000013467 fragmentation Methods 0.000 abstract 1
- 238000006062 fragmentation reaction Methods 0.000 abstract 1
- OFCRWKNWYKHWOS-UHFFFAOYSA-N hept-4-ynal Chemical compound CCC#CCCC=O OFCRWKNWYKHWOS-UHFFFAOYSA-N 0.000 abstract 1
- DQNOBCJGUXBBBF-UHFFFAOYSA-N hept-5-ynal Chemical compound CC#CCCCC=O DQNOBCJGUXBBBF-UHFFFAOYSA-N 0.000 abstract 1
- JIBLCOIURXDOGU-UHFFFAOYSA-N hex-5-ynal Chemical compound O=CCCCC#C JIBLCOIURXDOGU-UHFFFAOYSA-N 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 abstract 1
- RVRRJEYBQUYSPP-UHFFFAOYSA-N pentadec-4-ynal Chemical compound C(CCC#CCCCCCCCCCC)=O RVRRJEYBQUYSPP-UHFFFAOYSA-N 0.000 abstract 1
- 238000005502 peroxidation Methods 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- BYMWJSOFNAEWSR-UHFFFAOYSA-N undec-4-ynal Chemical compound CCCCCCC#CCCC=O BYMWJSOFNAEWSR-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D203/00—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom
- C07D203/04—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D203/06—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D203/22—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/56—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds
- C07C45/57—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom
- C07C45/58—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom in three-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/222—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms with only carbon-to-carbon triple bonds as unsaturation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/225—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D203/00—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom
- C07D203/26—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/32—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by aldehydo- or ketonic radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
- C07J71/0005—Oxygen-containing hetero ring
- C07J71/001—Oxiranes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1401468A CH503678A (de) | 1966-11-01 | 1968-09-19 | Verfahren zur Herstellung von Acetylenverbindungen |
DE19691951103 DE1951103A1 (de) | 1968-09-19 | 1969-10-10 | Verfahren zur Herstellung von Aldehyden |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1257111A true GB1257111A (enrdf_load_stackoverflow) | 1971-12-15 |
Family
ID=25713479
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1257111D Expired GB1257111A (enrdf_load_stackoverflow) | 1968-09-19 | 1969-09-11 |
Country Status (4)
Country | Link |
---|---|
DE (1) | DE1951103A1 (enrdf_load_stackoverflow) |
FR (1) | FR2019463A6 (enrdf_load_stackoverflow) |
GB (1) | GB1257111A (enrdf_load_stackoverflow) |
NL (1) | NL6914176A (enrdf_load_stackoverflow) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4052422A (en) * | 1974-11-08 | 1977-10-04 | E. R. Squibb & Sons, Inc. | 4,5-secopregnane derivatives |
US4127589A (en) | 1974-11-08 | 1978-11-28 | E. R. Squibb & Sons, Inc. | 4,5-Seco-steroids |
US4235824A (en) * | 1976-07-27 | 1980-11-25 | Naarden International N.V. | Method for the preparation of fragrances, and method for the preparation of perfume compositions |
-
1969
- 1969-09-11 GB GB1257111D patent/GB1257111A/en not_active Expired
- 1969-09-16 FR FR6931496A patent/FR2019463A6/fr not_active Expired
- 1969-09-18 NL NL6914176A patent/NL6914176A/xx unknown
- 1969-10-10 DE DE19691951103 patent/DE1951103A1/de active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4052422A (en) * | 1974-11-08 | 1977-10-04 | E. R. Squibb & Sons, Inc. | 4,5-secopregnane derivatives |
US4127589A (en) | 1974-11-08 | 1978-11-28 | E. R. Squibb & Sons, Inc. | 4,5-Seco-steroids |
US4235824A (en) * | 1976-07-27 | 1980-11-25 | Naarden International N.V. | Method for the preparation of fragrances, and method for the preparation of perfume compositions |
Also Published As
Publication number | Publication date |
---|---|
FR2019463A6 (enrdf_load_stackoverflow) | 1970-07-03 |
NL6914176A (enrdf_load_stackoverflow) | 1970-03-23 |
DE1951103A1 (de) | 1971-04-29 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed [section 19, patents act 1949] | ||
PCNP | Patent ceased through non-payment of renewal fee |