JPS6225134B2 - - Google Patents

Info

Publication number: JPS6225134B2
Authority: JP; Japan
Prior art keywords: cis; trans; type; formula; carbon atoms
Prior art date: 1979-11-02
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

Application number

JP54142421A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5665843A (en

Inventor

Shuji Tsucha

Hideo Suzuki

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Nissan Chemical Corp

Original Assignee

Nissan Chemical Corp

Priority date (The priority date 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 date listed.)

1979-11-02

Filing date

1979-11-02

Publication date

1987-06-01

1979-11-02 Application filed by Nissan Chemical Corp filed Critical Nissan Chemical Corp

1979-11-02 Priority to JP14242179A priority Critical patent/JPS5665843A/ja

1980-05-23 Priority to US06/152,819 priority patent/US4338170A/en

1980-06-05 Priority to NL8003281A priority patent/NL8003281A/nl

1980-06-13 Priority to DE19803022296 priority patent/DE3022296A1/de

1980-06-13 Priority to GB8019391A priority patent/GB2054561B/en

1981-06-03 Publication of JPS5665843A publication Critical patent/JPS5665843A/ja

1987-06-01 Publication of JPS6225134B2 publication Critical patent/JPS6225134B2/ja

Status Granted legal-status Critical Current

Links

238000006243 chemical reaction Methods 0.000 claims description 19
239000003054 catalyst Substances 0.000 claims description 15
150000002148 esters Chemical class 0.000 claims description 14
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 13
238000000034 method Methods 0.000 claims description 12
-1 aromatic thiols Chemical class 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 8
150000002019 disulfides Chemical class 0.000 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 7
239000003999 initiator Substances 0.000 claims description 6
238000006317 isomerization reaction Methods 0.000 claims description 6
125000001183 hydrocarbyl group Chemical group 0.000 claims description 5
229920006395 saturated elastomer Chemical group 0.000 claims description 5
239000011261 inert gas Substances 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 3
229930195734 saturated hydrocarbon Chemical group 0.000 claims description 3
229930195735 unsaturated hydrocarbon Chemical group 0.000 claims description 3
ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 claims description 2
150000001356 alkyl thiols Chemical class 0.000 claims description 2
238000010438 heat treatment Methods 0.000 claims description 2
239000000203 mixture Substances 0.000 claims description 2
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 8
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 6
HIGQPQRQIQDZMP-DHZHZOJOSA-N Neryl acetate Natural products CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 6
HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 6
RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 6
238000007697 cis-trans-isomerization reaction Methods 0.000 description 5
239000002994 raw material Substances 0.000 description 5
239000002904 solvent Substances 0.000 description 5
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
BYCHQEILESTMQU-UHFFFAOYSA-N Propionsaeure-nerylester Natural products CCC(=O)OCC=C(C)CCC=C(C)C BYCHQEILESTMQU-UHFFFAOYSA-N 0.000 description 3
ARVSCQUZFFSNKF-NTCAYCPXSA-N [(2e)-3,7-dimethylocta-2,6-dienyl] hexanoate Chemical compound CCCCCC(=O)OC\C=C(/C)CCC=C(C)C ARVSCQUZFFSNKF-NTCAYCPXSA-N 0.000 description 3
HIGQPQRQIQDZMP-FLIBITNWSA-N neryl acetate Chemical compound CC(C)=CCC\C(C)=C/COC(C)=O HIGQPQRQIQDZMP-FLIBITNWSA-N 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
WCASXYBKJHWFMY-NSCUHMNNSA-N 2-Buten-1-ol Chemical compound C\C=C\CO WCASXYBKJHWFMY-NSCUHMNNSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
239000004342 Benzoyl peroxide Substances 0.000 description 2
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
BLUHKGOSFDHHGX-UHFFFAOYSA-N Phytol Natural products CC(C)CCCC(C)CCCC(C)CCCC(C)C=CO BLUHKGOSFDHHGX-UHFFFAOYSA-N 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
BOTWFXYSPFMFNR-OALUTQOASA-N all-rac-phytol Natural products CC(C)CCC[C@H](C)CCC[C@H](C)CCCC(C)=CCO BOTWFXYSPFMFNR-OALUTQOASA-N 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
235000019400 benzoyl peroxide Nutrition 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
YUIDGONLMDUWNF-UHFFFAOYSA-N ethyl 3-chloro-4h-thieno[3,2-b]pyrrole-5-carboxylate Chemical compound S1C=C(Cl)C2=C1C=C(C(=O)OCC)N2 YUIDGONLMDUWNF-UHFFFAOYSA-N 0.000 description 2
125000005842 heteroatom Chemical group 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
229910052723 transition metal Inorganic materials 0.000 description 2
150000003624 transition metals Chemical class 0.000 description 2
CRDAMVZIKSXKFV-FBXUGWQNSA-N (2-cis,6-cis)-farnesol Chemical compound CC(C)=CCC\C(C)=C/CC\C(C)=C/CO CRDAMVZIKSXKFV-FBXUGWQNSA-N 0.000 description 1
239000000260 (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol Substances 0.000 description 1
239000001707 (E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol Substances 0.000 description 1
JGMYDQCXGIMHLL-WAYWQWQTSA-N (Z)-hexadec-11-enoic acid Chemical compound CCCC\C=C/CCCCCCCCCC(O)=O JGMYDQCXGIMHLL-WAYWQWQTSA-N 0.000 description 1
BOTWFXYSPFMFNR-HMMYKYKNSA-N (e)-3,7,11,15-tetramethylhexadec-2-en-1-ol Chemical compound CC(C)CCCC(C)CCCC(C)CCC\C(C)=C\CO BOTWFXYSPFMFNR-HMMYKYKNSA-N 0.000 description 1
AROCLDYPZXMJPW-UHFFFAOYSA-N 1-(octyldisulfanyl)octane Chemical compound CCCCCCCCSSCCCCCCCC AROCLDYPZXMJPW-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
PWOBDMNCYMQTCE-UHFFFAOYSA-N 2-chlorobenzenethiol Chemical compound SC1=CC=CC=C1Cl PWOBDMNCYMQTCE-UHFFFAOYSA-N 0.000 description 1
229930008411 3,7-dimethylocta-2,6-dien-1-ol Natural products 0.000 description 1
YNWSTXBQNLCEPJ-UHFFFAOYSA-N 3-decyl-3h-dithiole Chemical compound CCCCCCCCCCC1SSC=C1 YNWSTXBQNLCEPJ-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
WVDYBOADDMMFIY-UHFFFAOYSA-N Cyclopentanethiol Chemical compound SC1CCCC1 WVDYBOADDMMFIY-UHFFFAOYSA-N 0.000 description 1
BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 1
239000005792 Geraniol Substances 0.000 description 1
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
GLZPCOQZEFWAFX-JXMROGBWSA-N Nerol Natural products CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 description 1
HNZBNQYXWOLKBA-UHFFFAOYSA-N Tetrahydrofarnesol Natural products CC(C)CCCC(C)CCCC(C)=CCO HNZBNQYXWOLKBA-UHFFFAOYSA-N 0.000 description 1
235000011054 acetic acid Nutrition 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000012670 alkaline solution Substances 0.000 description 1
YIYBQIKDCADOSF-UHFFFAOYSA-N alpha-Butylen-alpha-carbonsaeure Natural products CCC=CC(O)=O YIYBQIKDCADOSF-UHFFFAOYSA-N 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
229910052728 basic metal Inorganic materials 0.000 description 1
150000003818 basic metals Chemical class 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
CMKBCTPCXZNQKX-UHFFFAOYSA-N cyclohexanethiol Chemical compound SC1CCCCC1 CMKBCTPCXZNQKX-UHFFFAOYSA-N 0.000 description 1
230000018044 dehydration Effects 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
238000004821 distillation Methods 0.000 description 1
DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Natural products CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
229940043259 farnesol Drugs 0.000 description 1
229930002886 farnesol Natural products 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
WCASXYBKJHWFMY-UHFFFAOYSA-N gamma-methylallyl alcohol Natural products CC=CCO WCASXYBKJHWFMY-UHFFFAOYSA-N 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
229940113087 geraniol Drugs 0.000 description 1
239000001307 helium Substances 0.000 description 1
229910052734 helium Inorganic materials 0.000 description 1
SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
150000004678 hydrides Chemical class 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
BOTWFXYSPFMFNR-PYDDKJGSSA-N phytol Chemical compound CC(C)CCC[C@@H](C)CCC[C@@H](C)CCC\C(C)=C\CO BOTWFXYSPFMFNR-PYDDKJGSSA-N 0.000 description 1
235000019260 propionic acid Nutrition 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
230000035484 reaction time Effects 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
238000000926 separation method Methods 0.000 description 1
238000001577 simple distillation Methods 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
YIYBQIKDCADOSF-ONEGZZNKSA-N trans-pent-2-enoic acid Chemical compound CC\C=C\C(O)=O YIYBQIKDCADOSF-ONEGZZNKSA-N 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1

Classifications

- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

JP14242179A 1979-06-14 1979-11-02 Isomerization of beta-gamma unsaturated ester Granted JPS5665843A (en)

Priority Applications (5)

Application Number	Priority Date	Filing Date	Title
JP14242179A JPS5665843A (en)	1979-11-02	1979-11-02	Isomerization of beta-gamma unsaturated ester
US06/152,819 US4338170A (en)	1979-06-14	1980-05-23	Isomerization of β-γ-unsaturated alcohol or its ester
NL8003281A NL8003281A (nl)	1979-06-14	1980-06-05	Werkwijze voor het uitvoeren van een isomerisatie van een onverzadigde alkohol of een ester hiervan.
DE19803022296 DE3022296A1 (de)	1979-06-14	1980-06-13	Isomerisation von beta , gamma -ungesaettigtem alkohol oder dessen ester
GB8019391A GB2054561B (en)	1979-06-14	1980-06-13	Isomerization of y-unsaturated alcohol or its ester

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP14242179A JPS5665843A (en)	1979-11-02	1979-11-02	Isomerization of beta-gamma unsaturated ester

Publications (2)

Publication Number	Publication Date
JPS5665843A JPS5665843A (en)	1981-06-03
JPS6225134B2 true JPS6225134B2 (cs)	1987-06-01

Family

ID=15314931

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP14242179A Granted JPS5665843A (en)	1979-06-14	1979-11-02	Isomerization of beta-gamma unsaturated ester

Country Status (1)

Country	Link
JP (1)	JPS5665843A (cs)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EA028500B1 (ru) *	2012-12-18	2017-11-30	ДСМ АйПи АССЕТС Б.В.	Политиолы в качестве катализаторов цис/транс-изомеризации ненасыщенных соединений

1979
- 1979-11-02 JP JP14242179A patent/JPS5665843A/ja active Granted

Also Published As

Publication number	Publication date
JPS5665843A (en)	1981-06-03

Publication	Publication Date	Title
KR920004433A (ko)	1992-03-27	중합 제조방법
KR910011720A (ko)	1991-08-07	Cu-Al-X 촉매를 사용한 수소화 방법
US5973200A (en)	1999-10-26	Process for the preparation of 2-hydroxy-4-(methylthio) butanoic acid or methionine by mercaptan addition
US4529815A (en)	1985-07-16	Preparation of 4-pentenoates
JPH05170700A (ja)	1993-07-09	ビニル誘導体の製造方法
US4277623A (en)	1981-07-07	Conversion of alkane and/or cycloalkane thiols to disulfide with catalyst system comprised of cobalt molybdate and an alkali- or alkaline earth metal hydroxide
JPS6225134B2 (cs)	1987-06-01
US3574766A (en)	1971-04-13	Process for the production of beta-methylmercaptopropionaldehyde
US4889950A (en)	1989-12-26	Preparation of carboxylic esters
US2947779A (en)	1960-08-02	Process for the esterification of unsatureated acids
SE7705362L (sv)	1977-11-11	Sett for framstellning av 2-(amylbensoyl)bensoesyra
US3974207A (en)	1976-08-10	Method for producing methacrylic esters
JPS6310687B2 (cs)	1988-03-08
US4338170A (en)	1982-07-06	Isomerization of β-γ-unsaturated alcohol or its ester
US3994979A (en)	1976-11-30	Disulfide process
JPS6257608B2 (cs)	1987-12-02
Mondal et al.	1974	A novel synthesis of vinyl esters from vinylversatate-10
EP0782566A1 (en)	1997-07-09	Compositions containing pentaerythritol tetraesters and process for production thereof
JPH08119924A (ja)	1996-05-14	３，７−ジメチル−２，６−オクタジエンニトリルの異性化方法
GB934917A (en)	1963-08-21	Production of carboxylic acid esters of tertiary alcohols
JPS6230971B2 (cs)	1987-07-06
CA2019769C (en)	1999-01-26	S-alkylthiopropionic acids and derivatives
US3013038A (en)	1961-12-12	Conversion of acids to alcohols having one less carbon atom and esters thereof
Kabalka et al.	1993	Oxidative Deselenylation with Sodium Perborate and Sodium Percarbonate
ES476885A1 (es)	1979-05-16	Procedimiento de preparacion de esteres etilicos de acidos -carboxilicos.