NO791937L - Pyrrol- og pyrrolidin-karboksylsyrederivater for anvendelse som mellomprodukter, og fremgangsmaate for fremstilling derav - Google Patents
Pyrrol- og pyrrolidin-karboksylsyrederivater for anvendelse som mellomprodukter, og fremgangsmaate for fremstilling deravInfo
- Publication number
- NO791937L NO791937L NO791937A NO791937A NO791937L NO 791937 L NO791937 L NO 791937L NO 791937 A NO791937 A NO 791937A NO 791937 A NO791937 A NO 791937A NO 791937 L NO791937 L NO 791937L
- Authority
- NO
- Norway
- Prior art keywords
- oxo
- ethyl
- carboxylic acid
- stated
- carboxylate
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 10
- NYCVCXMSZNOGDH-UHFFFAOYSA-N pyrrolidine-1-carboxylic acid Chemical class OC(=O)N1CCCC1 NYCVCXMSZNOGDH-UHFFFAOYSA-N 0.000 title claims description 7
- 238000004519 manufacturing process Methods 0.000 title description 5
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 title description 4
- 239000013067 intermediate product Substances 0.000 title description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 34
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 29
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 24
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 19
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Substances C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 15
- 239000000243 solution Substances 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 238000002360 preparation method Methods 0.000 claims description 11
- 239000002904 solvent Substances 0.000 claims description 11
- 239000000543 intermediate Substances 0.000 claims description 7
- 238000010992 reflux Methods 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 239000007853 buffer solution Substances 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 150000002576 ketones Chemical class 0.000 claims description 4
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 239000001632 sodium acetate Substances 0.000 claims description 3
- 235000017281 sodium acetate Nutrition 0.000 claims description 3
- 238000003786 synthesis reaction Methods 0.000 claims description 3
- 239000008351 acetate buffer Substances 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N alpha-methyl toluene Natural products CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- YVHSJXQPSCUBBM-UHFFFAOYSA-N ethyl 3-oxo-4-(3-oxobutyl)pyrrolidine-1-carboxylate Chemical group CCOC(=O)N1CC(CCC(C)=O)C(=O)C1 YVHSJXQPSCUBBM-UHFFFAOYSA-N 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 8
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 4
- -1 alkali metal acetate Chemical class 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 6
- 150000002431 hydrogen Chemical class 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000000862 absorption spectrum Methods 0.000 description 4
- 239000012299 nitrogen atmosphere Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 101150041968 CDC13 gene Proteins 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 3
- 150000002081 enamines Chemical class 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- KLTVSWGXIAYTHO-UHFFFAOYSA-N 1-Octen-3-one Chemical compound CCCCCC(=O)C=C KLTVSWGXIAYTHO-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- TUCNEACPLKLKNU-UHFFFAOYSA-N acetyl Chemical compound C[C]=O TUCNEACPLKLKNU-UHFFFAOYSA-N 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- DQYGBMLEVQLDQC-UHFFFAOYSA-N ethyl 3-oxopyrrolidine-1-carboxylate Chemical compound CCOC(=O)N1CCC(=O)C1 DQYGBMLEVQLDQC-UHFFFAOYSA-N 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- FDDQRDMHICUGQC-UHFFFAOYSA-N pyrrole-1-carboxylic acid Chemical class OC(=O)N1C=CC=C1 FDDQRDMHICUGQC-UHFFFAOYSA-N 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000005594 diketone group Chemical group 0.000 description 1
- MKJDTCRQHSIGKX-UHFFFAOYSA-N ethyl 3-oxo-2,4-bis(3-oxobutyl)pyrrolidine-1-carboxylate Chemical compound CCOC(=O)N1CC(CCC(C)=O)C(=O)C1CCC(C)=O MKJDTCRQHSIGKX-UHFFFAOYSA-N 0.000 description 1
- LFSCJMYCDUTGLX-UHFFFAOYSA-N ethyl 3-oxo-4-(3-oxooctyl)pyrrolidine-1-carboxylate Chemical compound CCCCCC(=O)CCC1CN(C(=O)OCC)CC1=O LFSCJMYCDUTGLX-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000000411 inducer Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- OIWBNCGEFFHTNG-UHFFFAOYSA-N oct-1-yn-3-one Chemical compound CCCCCC(=O)C#C OIWBNCGEFFHTNG-UHFFFAOYSA-N 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/273—2-Pyrrolidones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyrrole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7817424A FR2428641A1 (fr) | 1978-06-12 | 1978-06-12 | Nouveaux derives d'acides pyrrole-1 et pyrrolidine-1 carboxyliques ainsi que leur procede de preparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO791937L true NO791937L (no) | 1979-12-13 |
Family
ID=9209345
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO791937A NO791937L (no) | 1978-06-12 | 1979-06-11 | Pyrrol- og pyrrolidin-karboksylsyrederivater for anvendelse som mellomprodukter, og fremgangsmaate for fremstilling derav |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4299768A (it) |
| JP (1) | JPS5540663A (it) |
| BE (1) | BE876786A (it) |
| CA (1) | CA1121823A (it) |
| CH (1) | CH640532A5 (it) |
| DD (1) | DD144262A5 (it) |
| DE (1) | DE2923697A1 (it) |
| DK (1) | DK241679A (it) |
| ES (1) | ES481486A1 (it) |
| FR (1) | FR2428641A1 (it) |
| GB (1) | GB2023585B (it) |
| HU (1) | HU180258B (it) |
| IT (1) | IT1121530B (it) |
| NL (1) | NL7904560A (it) |
| NO (1) | NO791937L (it) |
| PL (1) | PL118131B1 (it) |
| SE (1) | SE439161B (it) |
| SU (1) | SU843737A3 (it) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4127796A1 (de) * | 1991-08-22 | 1993-02-25 | Iro Ab | Faden-fournisseur |
| CN103044418B (zh) * | 2011-10-14 | 2015-02-04 | 上海朴颐化学科技有限公司 | (s,s)-2,8-二氮杂双环[4,3,0]壬烷的不对称合成方法、相关原料及制备方法 |
| CN104277036B (zh) * | 2013-07-02 | 2016-12-28 | 上海朴颐化学科技有限公司 | 一种(4aS,7aS)‑八氢‑1H‑吡咯并[3,4‑b]吡啶的纯化方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3060194A (en) * | 1960-03-29 | 1962-10-23 | American Cyanamid Co | 4-cyano-3-oxo-pyrrolidine carboxylates |
-
1978
- 1978-06-12 FR FR7817424A patent/FR2428641A1/fr active Granted
-
1979
- 1979-05-30 IT IT23119/79A patent/IT1121530B/it active
- 1979-06-06 BE BE0/195583A patent/BE876786A/xx not_active IP Right Cessation
- 1979-06-07 GB GB7919834A patent/GB2023585B/en not_active Expired
- 1979-06-09 PL PL1979216217A patent/PL118131B1/pl unknown
- 1979-06-11 DK DK241679A patent/DK241679A/da unknown
- 1979-06-11 HU HU79LA959A patent/HU180258B/hu unknown
- 1979-06-11 CH CH544779A patent/CH640532A5/fr not_active IP Right Cessation
- 1979-06-11 NL NL7904560A patent/NL7904560A/xx not_active Application Discontinuation
- 1979-06-11 US US06/047,585 patent/US4299768A/en not_active Expired - Lifetime
- 1979-06-11 CA CA000329513A patent/CA1121823A/en not_active Expired
- 1979-06-11 NO NO791937A patent/NO791937L/no unknown
- 1979-06-11 SE SE7905060A patent/SE439161B/sv not_active IP Right Cessation
- 1979-06-12 ES ES481486A patent/ES481486A1/es not_active Expired
- 1979-06-12 SU SU792775352A patent/SU843737A3/ru active
- 1979-06-12 DD DD79213563A patent/DD144262A5/de unknown
- 1979-06-12 JP JP7453079A patent/JPS5540663A/ja active Granted
- 1979-06-12 DE DE19792923697 patent/DE2923697A1/de not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| ES481486A1 (es) | 1980-07-01 |
| JPS5540663A (en) | 1980-03-22 |
| PL118131B1 (en) | 1981-09-30 |
| SE7905060L (sv) | 1979-12-13 |
| NL7904560A (nl) | 1979-12-14 |
| FR2428641A1 (fr) | 1980-01-11 |
| DK241679A (da) | 1979-12-13 |
| IT1121530B (it) | 1986-04-02 |
| HU180258B (en) | 1983-02-28 |
| US4299768A (en) | 1981-11-10 |
| GB2023585A (en) | 1980-01-03 |
| CH640532A5 (fr) | 1984-01-13 |
| JPS6340186B2 (it) | 1988-08-10 |
| PL216217A1 (it) | 1980-07-01 |
| DE2923697A1 (de) | 1979-12-20 |
| IT7923119A0 (it) | 1979-05-30 |
| BE876786A (fr) | 1979-12-06 |
| DD144262A5 (de) | 1980-10-08 |
| SE439161B (sv) | 1985-06-03 |
| FR2428641B1 (it) | 1981-04-17 |
| GB2023585B (en) | 1982-10-13 |
| SU843737A3 (ru) | 1981-06-30 |
| CA1121823A (en) | 1982-04-13 |
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