JPS6265687A - 光学活性（ｒ）−２−ハロ−１−フエニルエタノ−ルの製造法 - Google Patents
光学活性（ｒ）−２−ハロ−１−フエニルエタノ−ルの製造法Info
- Publication number
- JPS6265687A JPS6265687A JP20364485A JP20364485A JPS6265687A JP S6265687 A JPS6265687 A JP S6265687A JP 20364485 A JP20364485 A JP 20364485A JP 20364485 A JP20364485 A JP 20364485A JP S6265687 A JPS6265687 A JP S6265687A
- Authority
- JP
- Japan
- Prior art keywords
- genus
- phenylethanol
- formula
- halo
- formulas
- 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.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 244000005700 microbiome Species 0.000 claims abstract description 18
- 241001149669 Hanseniaspora Species 0.000 claims abstract description 7
- 241000235003 Saccharomycopsis Species 0.000 claims abstract description 7
- 241001638540 Arthroascus Species 0.000 claims abstract description 5
- 241001149698 Lipomyces Species 0.000 claims abstract description 5
- 125000005843 halogen group Chemical group 0.000 claims abstract description 4
- 241000336534 Chlamydomyces Species 0.000 claims abstract description 3
- 241000235648 Pichia Species 0.000 claims abstract 3
- 230000003287 optical effect Effects 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 8
- 241000222356 Coriolus Species 0.000 claims description 5
- 241000221960 Neurospora Species 0.000 claims description 4
- 241000235389 Absidia Species 0.000 claims description 3
- 241000235395 Mucor Species 0.000 claims description 3
- 241000196250 Prototheca Species 0.000 claims description 3
- 241001480014 Trigonopsis Species 0.000 claims description 3
- 241001450911 Circinella Species 0.000 claims description 2
- 241001231443 Circinella simplex Species 0.000 claims description 2
- 241000235649 Kluyveromyces Species 0.000 claims description 2
- 235000014663 Kluyveromyces fragilis Nutrition 0.000 claims description 2
- 241001287972 Microthecium Species 0.000 claims description 2
- WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 claims 1
- 241000336535 Chlamydomyces palmarum Species 0.000 claims 1
- 241000235650 Kluyveromyces marxianus Species 0.000 claims 1
- 241000235527 Rhizopus Species 0.000 claims 1
- 241001264639 Vetulina Species 0.000 claims 1
- XPNGNIFUDRPBFJ-UHFFFAOYSA-N alpha-methylbenzylalcohol Natural products CC1=CC=CC=C1CO XPNGNIFUDRPBFJ-UHFFFAOYSA-N 0.000 claims 1
- 239000012528 membrane Substances 0.000 claims 1
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 abstract description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 4
- 239000003814 drug Substances 0.000 abstract description 4
- 241000221207 Filobasidium Species 0.000 abstract description 2
- 241001465754 Metazoa Species 0.000 abstract description 2
- 241000235575 Mortierella Species 0.000 abstract description 2
- 229940079593 drug Drugs 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract description 2
- 241000908198 Actinomucor Species 0.000 abstract 1
- 241001508809 Ambrosiozyma Species 0.000 abstract 1
- 239000003905 agrochemical Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- -1 ethanol compound Chemical class 0.000 abstract 1
- 230000000813 microbial effect Effects 0.000 abstract 1
- 239000002304 perfume Substances 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
- 238000006243 chemical reaction Methods 0.000 description 15
- IMACFCSSMIZSPP-UHFFFAOYSA-N phenacyl chloride Chemical compound ClCC(=O)C1=CC=CC=C1 IMACFCSSMIZSPP-UHFFFAOYSA-N 0.000 description 6
- 230000001580 bacterial effect Effects 0.000 description 5
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
- 229930006000 Sucrose Natural products 0.000 description 4
- 238000005119 centrifugation Methods 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 235000015097 nutrients Nutrition 0.000 description 4
- 239000005720 sucrose Substances 0.000 description 4
- XWCQSILTDPAWDP-QMMMGPOBSA-N (1r)-2-chloro-1-phenylethanol Chemical compound ClC[C@H](O)C1=CC=CC=C1 XWCQSILTDPAWDP-QMMMGPOBSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 239000008103 glucose Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- LIGACIXOYTUXAW-UHFFFAOYSA-N phenacyl bromide Chemical compound BrCC(=O)C1=CC=CC=C1 LIGACIXOYTUXAW-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 2
- PJGLCPCTOMLEFG-UHFFFAOYSA-N 1-chloro-1-phenylethanol Chemical compound CC(O)(Cl)C1=CC=CC=C1 PJGLCPCTOMLEFG-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- 229940041514 candida albicans extract Drugs 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000008363 phosphate buffer Substances 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000012138 yeast extract Substances 0.000 description 2
- 240000005007 Actinomucor elegans Species 0.000 description 1
- 235000013650 Actinomucor elegans Nutrition 0.000 description 1
- 241000159515 Ambrosiozyma philentoma Species 0.000 description 1
- 241000908171 Backusella circina Species 0.000 description 1
- 241001341614 Basidiobolus meristosporus Species 0.000 description 1
- 241001508787 Citeromyces Species 0.000 description 1
- 241001508786 Citeromyces matritensis Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 241000033325 Cystofilobasidium macerans Species 0.000 description 1
- 244000285963 Kluyveromyces fragilis Species 0.000 description 1
- 241000144128 Lichtheimia corymbifera Species 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 241001644966 Microthecium compressum Species 0.000 description 1
- 241000498617 Mucor javanicus Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000196248 Prototheca zopfii Species 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 241000235346 Schizosaccharomyces Species 0.000 description 1
- 241000235347 Schizosaccharomyces pombe Species 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 241000096008 Thamnostylum nigricans Species 0.000 description 1
- JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 description 1
- 241000276425 Xiphophorus maculatus Species 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 235000020958 biotin Nutrition 0.000 description 1
- 229960002685 biotin Drugs 0.000 description 1
- 239000011616 biotin Substances 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 229910000366 copper(II) sulfate Inorganic materials 0.000 description 1
- 238000012136 culture method Methods 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012156 elution solvent Substances 0.000 description 1
- ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000003100 immobilizing effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 229910000357 manganese(II) sulfate Inorganic materials 0.000 description 1
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 125000001297 nitrogen containing inorganic group Chemical group 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 235000019157 thiamine Nutrition 0.000 description 1
- KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 description 1
- 229960003495 thiamine Drugs 0.000 description 1
- 239000011721 thiamine Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 239000011686 zinc sulphate Substances 0.000 description 1
- 235000009529 zinc sulphate Nutrition 0.000 description 1
Landscapes
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20364485A JPS6265687A (ja) | 1985-09-14 | 1985-09-14 | 光学活性（ｒ）−２−ハロ−１−フエニルエタノ−ルの製造法 |
| US06/849,985 US4857468A (en) | 1985-04-13 | 1986-04-10 | Process for preparing optically active 2-halo-1-phenyl ethanol |
| EP86104993A EP0198440B1 (en) | 1985-04-13 | 1986-04-11 | Process for preparing optically active 2-halo-1-phenyl ethanol |
| DE8686104993T DE3686502T2 (de) | 1985-04-13 | 1986-04-11 | Verfahren zur herstellung von optisch aktivem 2-halo-phenyl-ethanol. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20364485A JPS6265687A (ja) | 1985-09-14 | 1985-09-14 | 光学活性（ｒ）−２−ハロ−１−フエニルエタノ−ルの製造法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6265687A true JPS6265687A (ja) | 1987-03-24 |
| JPH0528111B2 JPH0528111B2 (enrdf_load_stackoverflow) | 1993-04-23 |
Family
ID=16477456
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20364485A Granted JPS6265687A (ja) | 1985-04-13 | 1985-09-14 | 光学活性（ｒ）−２−ハロ−１−フエニルエタノ−ルの製造法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6265687A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10248277A1 (de) * | 2002-10-16 | 2004-05-06 | X-Zyme Gmbh | Verfahren zur Herstellung optisch aktiver Verbindungen |
-
1985
- 1985-09-14 JP JP20364485A patent/JPS6265687A/ja active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10248277A1 (de) * | 2002-10-16 | 2004-05-06 | X-Zyme Gmbh | Verfahren zur Herstellung optisch aktiver Verbindungen |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0528111B2 (enrdf_load_stackoverflow) | 1993-04-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH0516833B2 (enrdf_load_stackoverflow) | ||
| EP0317998B1 (en) | Manufacturing method of optically-active 1,2-diols | |
| FR2461753A1 (fr) | Procede de preparation d'une cephalosporine par fermentation et micro-organisme destine a la mise en oeuvre de ce procede | |
| JPS6265687A (ja) | 光学活性（ｒ）−２−ハロ−１−フエニルエタノ−ルの製造法 | |
| JPS6312288A (ja) | 光学活性（ｒ）−４−フエニル−２−ブタノ−ルの製造法 | |
| JPS6312287A (ja) | 光学活性（ｓ）−４−フエニル−２−ブタノ−ルの製造法 | |
| NL8006026A (nl) | Werkwijze voor het bereiden van d(-)-beta-hydroxyiso- boterzuur. | |
| JPS6229998A (ja) | 光学活性（ｒ）−２−ハロ−１−フエニルエタノ−ルの製造法 | |
| JP4475407B2 (ja) | 微生物を利用した光学活性３−クロロ−２−メチル−１，２−プロパンジオールの製造方法 | |
| KR20050072066A (ko) | 미생물을 이용한 광학 활성 3－클로로－2－메틸－1,2－프로판디올의 제조 방법 | |
| JPS6265686A (ja) | 光学活性（ｓ）−２−ハロ−１−フエニルエタノ−ルの製造法 | |
| JPS63251098A (ja) | （ｒ）−３−ハロゲノ−１，２−プロパンジオ−ルの製造法 | |
| JP3747640B2 (ja) | 光学活性１，２−ジオール環状炭酸エステルの製造法 | |
| JP2786500B2 (ja) | 光学活性１，３―ブタンジオールの製法 | |
| JPH0527382B2 (enrdf_load_stackoverflow) | ||
| JPH0231684A (ja) | 光学活性１，３―ブタンジオールの製造方法 | |
| JPS6112678B2 (enrdf_load_stackoverflow) | ||
| JPS5953838B2 (ja) | β−ヒドロキシ吉草酸の製造方法 | |
| JP3651924B2 (ja) | （ｒ）−４−（２−ハロ−１−ヒドロキシエチル）−２−トリフルオロメチルチアゾールの製造方法 | |
| JP2977885B2 (ja) | 微生物を利用した光学活性体の製造方法 | |
| JP3163388B2 (ja) | （ｓ）−１−フェニル−１，３−プロパンジオールの製造方法 | |
| JPH0521557B2 (enrdf_load_stackoverflow) | ||
| JP2761064B2 (ja) | 光学活性１，３―ブタンジオールの製法 | |
| WO2000023608A1 (en) | Preparation of amino alcohols | |
| JPS6363387A (ja) | （Ｒ）―γ―ブチロラクトン―γ―プロピオン酸エステルの製造方法 |