NO300544B1 - Nye organobor-forbindelser og fremgangsmåte ved fremstilling av usubstituerte propargylalkoholer - Google Patents
Nye organobor-forbindelser og fremgangsmåte ved fremstilling av usubstituerte propargylalkoholer Download PDFInfo
- Publication number
- NO300544B1 NO300544B1 NO934676A NO934676A NO300544B1 NO 300544 B1 NO300544 B1 NO 300544B1 NO 934676 A NO934676 A NO 934676A NO 934676 A NO934676 A NO 934676A NO 300544 B1 NO300544 B1 NO 300544B1
- Authority
- NO
- Norway
- Prior art keywords
- mmol
- tetrahydrofuran
- trisubstituted
- nonane
- trimethylsilyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 30
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- -1 Propargyl Alcohols Chemical class 0.000 title abstract description 28
- 150000001299 aldehydes Chemical class 0.000 claims abstract description 13
- 150000002576 ketones Chemical class 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 3
- 239000003153 chemical reaction reagent Substances 0.000 abstract description 16
- 238000003786 synthesis reaction Methods 0.000 abstract description 10
- 230000015572 biosynthetic process Effects 0.000 abstract description 9
- 238000002360 preparation method Methods 0.000 abstract description 7
- 239000000543 intermediate Substances 0.000 abstract description 6
- 229930014626 natural product Natural products 0.000 abstract description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical class C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 65
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 42
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 31
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 30
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 29
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 27
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- 238000003756 stirring Methods 0.000 description 23
- 239000002904 solvent Substances 0.000 description 21
- 238000005481 NMR spectroscopy Methods 0.000 description 20
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 16
- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 16
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 14
- 239000012074 organic phase Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- FEJUGLKDZJDVFY-UHFFFAOYSA-N 9-borabicyclo[3.3.1]nonane Substances C1CCC2CCCC1B2 FEJUGLKDZJDVFY-UHFFFAOYSA-N 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 239000007788 liquid Substances 0.000 description 11
- 239000000376 reactant Substances 0.000 description 10
- 238000010898 silica gel chromatography Methods 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 8
- 239000012300 argon atmosphere Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 8
- KUFWTXSQQKDMAI-UHFFFAOYSA-N ethynylsilicon Chemical group [Si]C#C KUFWTXSQQKDMAI-UHFFFAOYSA-N 0.000 description 7
- 229920006395 saturated elastomer Polymers 0.000 description 7
- 239000011780 sodium chloride Substances 0.000 description 7
- 239000006228 supernatant Substances 0.000 description 7
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 6
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 6
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 6
- 229910052744 lithium Inorganic materials 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 238000005192 partition Methods 0.000 description 5
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 4
- WGOAAZJLIYNALW-QWHCGFSZSA-N (3s,4r)-4-methoxy-4-methyl-1-trimethylsilyloct-1-yn-3-ol Chemical compound CCCC[C@@](C)(OC)[C@@H](O)C#C[Si](C)(C)C WGOAAZJLIYNALW-QWHCGFSZSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000000304 alkynyl group Chemical group 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 244000309464 bull Species 0.000 description 3
- 229960004132 diethyl ether Drugs 0.000 description 3
- 150000002148 esters Chemical group 0.000 description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 3
- 235000019341 magnesium sulphate Nutrition 0.000 description 3
- 229940094443 oxytocics prostaglandins Drugs 0.000 description 3
- 150000003180 prostaglandins Chemical class 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 3
- WGOAAZJLIYNALW-CHWSQXEVSA-N (3r,4r)-4-methoxy-4-methyl-1-trimethylsilyloct-1-yn-3-ol Chemical compound CCCC[C@@](C)(OC)[C@H](O)C#C[Si](C)(C)C WGOAAZJLIYNALW-CHWSQXEVSA-N 0.000 description 2
- OWQRSJQIENIBMT-VHSXEESVSA-N (3s,4r)-4-methoxy-4-methyloct-1-yn-3-ol Chemical compound CCCC[C@@](C)(OC)[C@@H](O)C#C OWQRSJQIENIBMT-VHSXEESVSA-N 0.000 description 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 2
- LHRITDPHGURSFT-UHFFFAOYSA-N 1-(2-trimethylsilylethynyl)cyclohexan-1-ol Chemical compound C[Si](C)(C)C#CC1(O)CCCCC1 LHRITDPHGURSFT-UHFFFAOYSA-N 0.000 description 2
- QYLFHLNFIHBCPR-UHFFFAOYSA-N 1-ethynylcyclohexan-1-ol Chemical compound C#CC1(O)CCCCC1 QYLFHLNFIHBCPR-UHFFFAOYSA-N 0.000 description 2
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 2
- VQUXVWMAXIQKTQ-UHFFFAOYSA-N 3-methylnon-1-yn-3-ol Chemical compound CCCCCCC(C)(O)C#C VQUXVWMAXIQKTQ-UHFFFAOYSA-N 0.000 description 2
- IBMLPAFABJTKSV-UHFFFAOYSA-N 4,4-dimethyl-1-trimethylsilylpent-1-yn-3-ol Chemical compound CC(C)(C)C(O)C#C[Si](C)(C)C IBMLPAFABJTKSV-UHFFFAOYSA-N 0.000 description 2
- ILPLTEOGHOQFHJ-UHFFFAOYSA-N 4,4-dimethylpent-1-yn-3-ol Chemical compound CC(C)(C)C(O)C#C ILPLTEOGHOQFHJ-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- 150000001345 alkine derivatives Chemical class 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 229910000085 borane Inorganic materials 0.000 description 2
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 2
- 235000021466 carotenoid Nutrition 0.000 description 2
- 150000001747 carotenoids Chemical class 0.000 description 2
- 239000002178 crystalline material Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 150000002617 leukotrienes Chemical class 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 150000003431 steroids Chemical class 0.000 description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N trihydridoboron Substances B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 2
- VMRZRELRFMMLLU-MRVPVSSYSA-N (2r)-2-methoxy-2-methylhexanal Chemical compound CCCC[C@@](C)(OC)C=O VMRZRELRFMMLLU-MRVPVSSYSA-N 0.000 description 1
- OWQRSJQIENIBMT-NXEZZACHSA-N (3r,4r)-4-methoxy-4-methyloct-1-yn-3-ol Chemical compound CCCC[C@@](C)(OC)[C@H](O)C#C OWQRSJQIENIBMT-NXEZZACHSA-N 0.000 description 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- MUXBHXBDEFJJQK-UHFFFAOYSA-N 1-borabicyclo[3.3.1]nonane Chemical compound C1CCC2CCCB1C2 MUXBHXBDEFJJQK-UHFFFAOYSA-N 0.000 description 1
- KGFXSPBJDFBTEO-UHFFFAOYSA-N 1-trimethylsilyldec-1-yn-3-ol Chemical compound CCCCCCCC(O)C#C[Si](C)(C)C KGFXSPBJDFBTEO-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 1
- BKMMTJMQCTUHRP-UHFFFAOYSA-N 2-aminopropan-1-ol Chemical compound CC(N)CO BKMMTJMQCTUHRP-UHFFFAOYSA-N 0.000 description 1
- SAPLWGOGHIZCRJ-UHFFFAOYSA-N 3-methyl-1-trimethylsilylnon-1-yn-3-ol Chemical compound CCCCCCC(C)(O)C#C[Si](C)(C)C SAPLWGOGHIZCRJ-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 1
- 241000276498 Pollachius virens Species 0.000 description 1
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
- YSVZGWAJIHWNQK-UHFFFAOYSA-N [3-(hydroxymethyl)-2-bicyclo[2.2.1]heptanyl]methanol Chemical compound C1CC2C(CO)C(CO)C1C2 YSVZGWAJIHWNQK-UHFFFAOYSA-N 0.000 description 1
- QQIRAVWVGBTHMJ-UHFFFAOYSA-N [dimethyl-(trimethylsilylamino)silyl]methane;lithium Chemical compound [Li].C[Si](C)(C)N[Si](C)(C)C QQIRAVWVGBTHMJ-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- WNTGVOIBBXFMLR-UHFFFAOYSA-N bicyclo[3.3.1]nonane Chemical compound C1CCC2CCCC1C2 WNTGVOIBBXFMLR-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- DQBUGZRLSSLUKC-UHFFFAOYSA-N dec-1-yn-3-ol Chemical compound CCCCCCCC(O)C#C DQBUGZRLSSLUKC-UHFFFAOYSA-N 0.000 description 1
- FAMGJMYDHOESPR-UHFFFAOYSA-M dilithium;carbanide;bromide Chemical compound [Li+].[Li+].[CH3-].[Br-] FAMGJMYDHOESPR-UHFFFAOYSA-M 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 description 1
- WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 150000002825 nitriles Chemical group 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 1
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical group C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/717,970 US5110966A (en) | 1991-06-20 | 1991-06-20 | New organoboron reagents for the preparation unsubstituted propargylic alcohols |
| PCT/US1992/004147 WO1993000347A1 (en) | 1991-06-20 | 1992-05-18 | New organoboron reagents for the preparation of unsubstituted propargylic alcohols |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO934676D0 NO934676D0 (no) | 1993-12-17 |
| NO934676L NO934676L (no) | 1993-12-17 |
| NO300544B1 true NO300544B1 (no) | 1997-06-16 |
Family
ID=24884271
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO934676A NO300544B1 (no) | 1991-06-20 | 1993-12-17 | Nye organobor-forbindelser og fremgangsmåte ved fremstilling av usubstituerte propargylalkoholer |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US5110966A (zh) |
| EP (1) | EP0589965B1 (zh) |
| JP (1) | JPH06508631A (zh) |
| KR (1) | KR100220877B1 (zh) |
| AT (1) | ATE147393T1 (zh) |
| AU (1) | AU659847B2 (zh) |
| CA (1) | CA2109954A1 (zh) |
| DE (1) | DE69216611T2 (zh) |
| DK (1) | DK0589965T3 (zh) |
| ES (1) | ES2099264T3 (zh) |
| FI (1) | FI103891B1 (zh) |
| GR (1) | GR3022417T3 (zh) |
| HU (1) | HU215087B (zh) |
| IE (1) | IE922006A1 (zh) |
| NO (1) | NO300544B1 (zh) |
| NZ (1) | NZ243155A (zh) |
| TW (1) | TW208016B (zh) |
| WO (1) | WO1993000347A1 (zh) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0308672D0 (en) * | 2003-04-15 | 2003-05-21 | Johnson Matthey Plc | Process |
| CN115806471A (zh) * | 2022-12-15 | 2023-03-17 | 延安大学 | 一种碱催化多聚甲醛与炔制备取代炔丙醇的制备方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4537773A (en) * | 1983-12-05 | 1985-08-27 | E. I. Du Pont De Nemours And Company | α-Aminoboronic acid derivatives |
| US4644075A (en) * | 1985-12-09 | 1987-02-17 | Massachusetts Institute Of Technology | Chiral borane reagents |
-
1991
- 1991-06-20 US US07/717,970 patent/US5110966A/en not_active Expired - Fee Related
-
1992
- 1992-05-18 DE DE69216611T patent/DE69216611T2/de not_active Expired - Fee Related
- 1992-05-18 AU AU19984/92A patent/AU659847B2/en not_active Ceased
- 1992-05-18 HU HU9303645A patent/HU215087B/hu not_active IP Right Cessation
- 1992-05-18 ES ES92912158T patent/ES2099264T3/es not_active Expired - Lifetime
- 1992-05-18 KR KR1019930703938A patent/KR100220877B1/ko not_active IP Right Cessation
- 1992-05-18 EP EP92912158A patent/EP0589965B1/en not_active Expired - Lifetime
- 1992-05-18 DK DK92912158.0T patent/DK0589965T3/da active
- 1992-05-18 WO PCT/US1992/004147 patent/WO1993000347A1/en active IP Right Grant
- 1992-05-18 CA CA002109954A patent/CA2109954A1/en not_active Abandoned
- 1992-05-18 AT AT92912158T patent/ATE147393T1/de active
- 1992-05-18 JP JP5501462A patent/JPH06508631A/ja active Pending
- 1992-06-16 TW TW081104709A patent/TW208016B/zh active
- 1992-06-16 NZ NZ243155A patent/NZ243155A/en unknown
- 1992-07-01 IE IE200692A patent/IE922006A1/en not_active Application Discontinuation
-
1993
- 1993-12-17 FI FI935699A patent/FI103891B1/fi active
- 1993-12-17 NO NO934676A patent/NO300544B1/no not_active IP Right Cessation
-
1997
- 1997-01-29 GR GR970400141T patent/GR3022417T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE69216611T2 (de) | 1997-05-22 |
| KR100220877B1 (ko) | 1999-10-01 |
| US5110966A (en) | 1992-05-05 |
| HU215087B (hu) | 1998-09-28 |
| WO1993000347A1 (en) | 1993-01-07 |
| FI935699A0 (fi) | 1993-12-17 |
| HU9303645D0 (en) | 1994-04-28 |
| DE69216611D1 (de) | 1997-02-20 |
| AU1998492A (en) | 1993-01-25 |
| EP0589965A1 (en) | 1994-04-06 |
| GR3022417T3 (en) | 1997-04-30 |
| HUT69764A (en) | 1995-09-28 |
| KR940701399A (ko) | 1994-05-28 |
| NZ243155A (en) | 1994-03-25 |
| NO934676D0 (no) | 1993-12-17 |
| NO934676L (no) | 1993-12-17 |
| IE922006A1 (en) | 1992-12-30 |
| EP0589965B1 (en) | 1997-01-08 |
| ES2099264T3 (es) | 1997-05-16 |
| JPH06508631A (ja) | 1994-09-29 |
| FI103891B (fi) | 1999-10-15 |
| ATE147393T1 (de) | 1997-01-15 |
| FI103891B1 (fi) | 1999-10-15 |
| TW208016B (zh) | 1993-06-21 |
| AU659847B2 (en) | 1995-06-01 |
| DK0589965T3 (da) | 1997-01-27 |
| CA2109954A1 (en) | 1993-01-07 |
| FI935699A (fi) | 1993-12-17 |
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