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1ChemInform Abstract: DIE HYDRIERUNG VON 1‐ALKYL(ARYL)THIO‐1‐BUTEN‐3‐IN AN PALLADIUM‐KATALYSATOREN

G. S. VASIL'EV,E. P. MIKOS,V. N. PETROV,B. D. POLKOVNIKOV,R. I. SHEKHTMAN,E. N. PRILEZHAEVA

AbstractDie cis‐ und trans‐Alkyl(Aryl)thio‐1‐buten‐3‐ine (I) lassen sich in Methanol über Palladium‐Katalysatoren, hergestellt durch Reduktion von Palladiumchlorid mit Natrium‐borhydrid, leicht zu Alkyl(Aryl)thio‐l ,3‐butadienen (II) hydrieren.

1971Chemischer Informationsdienst Organische Chemie

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2Hydrogenation Of L-Alkyl(Aryl)-Thiobuten-1-Ines-3 Over Palladium Catalyst

Gs Vasilev,Ep Mikos, Vn Petrov,Polkovni.Bd,Shekhtma.Ri,Prilezha.En

1971IZVESTIYA AKADEMII NAUK SSSR-SERIYA KHIMICHESKAYA

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3Hydrogenation of 1-Alkyl(aryl)thio-1-buten-3-ynes over Palladium Catalyst

G. S. Vasil'ev,É. P. Mikos,V. N. Petrov,B. D. Polkovnikov,R. I. Shekhtman,E. N. Prilezhaeva

A method was developed for the catalytic hydrogenation of the triple bond in 1-alkyl(aryl)thio-1-buten-3-ynes in order to obtain 1-alkylthio-1,3-butadienes.

1971Bulletin of the Academy of Sciences of the USSR, Division of chemical science（1971）

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4ChemInform Abstract: CYCLISCHE UNGESAETTIGTE VERBINDUNGEN 31. MITT. BEQUEME METHODE ZUR BESTIMMUNG DER KONFIGURATION VON SUBSTITUENTEN IN 7‐STELLUNG DES NORBORNEN‐SKELETTS

V. A. MIRONOV,B. D. POLKOVNIKOV,E. P. MIKOS,T. M. FADEEVA, A. A. ACHREM

Chemischer Informationsdienst. Organische ChemieVolume 1, Issue 21 Isocyclic Compounds ChemInform Abstract: CYCLISCHE UNGESAETTIGTE VERBINDUNGEN 31. MITT. BEQUEME METHODE ZUR BESTIMMUNG DER KONFIGURATION VON SUBSTITUENTEN IN 7-STELLUNG DES NORBORNEN-SKELETTS V. A. MIRONOV, Search for more papers by this authorB. D. POLKOVNIKOV, Search for more papers by this authorE. P. MIKOS, Search for more papers by this authorT. M. FADEEVA, Search for more papers by this authorA. A. ACHREM, Search for more papers by this author V. A. MIRONOV, Search for more papers by this authorB. D. POLKOVNIKOV, Search for more papers by this authorE. P. MIKOS, Search for more papers by this authorT. M. FADEEVA, Search for more papers by this authorA. A. ACHREM, Search for more papers by this author First published: May 26, 1970 https://doi.org/10.1002/chin.197021043Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinked InRedditWechat No abstract is available for this article. Volume1, Issue21May 26, 1970 RelatedInformation

1970Chemischer Informationsdienst Organische Chemie（1970）

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5Unsaturated Ring Compounds

V. A. Mironov,B. D. Polkovnikov,É. P. Mikos,T. M. Fadeeva,A. A. Akhrem

The hydrogenation kinetics of endo anhydrides of 7-syn-methyl-(II) and 7-anti-methyl-(III)-bicyclo [2,2,1]-hept-2-ene-5,6-dicarboxylic acids and the corresponding unsubstituted anhydride (I) have been in vestigated. Hydrogenation of the syn isomer (II) took place at approximately half the rate of the anti isomer (III) and the unsubstituted anhydride (I). The last two compounds gave approximately the same hydro genation rates.

1970Bulletin of the Academy of Sciences of the USSR, Division of chemical science（1970）

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6Cyclic Unsaturated Compounds .31. A Convenient Method For Determination Of Substitute Configuration In Position-7 Of Norbornene Skeleton