4-SUBSTITUTED-5-ALKYLIDENE-2-CYCLOPENTENONE AND ITS PREPARATION
NEW MATERIAL:The compound of formula I (R is 1-10C alkyl, ester, carboxyl, or its salt; R is 1-10C alkyl or alkenyl). EXAMPLE:4-(2-Octenyl)-5-(6-carbonyloxyhexylidene)-cyclopentenone methyl ester. USE:Pharmaceuticals. It has excellent carcinostatic and antiviral activities, and is useful as a carcin...
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| creator | NOGAMI JIYUNZOU KUROZUMI SEIJI |
| description | NEW MATERIAL:The compound of formula I (R is 1-10C alkyl, ester, carboxyl, or its salt; R is 1-10C alkyl or alkenyl). EXAMPLE:4-(2-Octenyl)-5-(6-carbonyloxyhexylidene)-cyclopentenone methyl ester. USE:Pharmaceuticals. It has excellent carcinostatic and antiviral activities, and is useful as a carcinostatic agent or a synthetic intermediate of known natural clavulone and claviridenone having strong carcinostatic activity. PREPARATION:The compound of formula I wherein R and R can be prepared by (1) reducing and eliminating the PhSO group of the sulfoxide compound of formula II (R is 1-10C alkyl or ester; R is OH-protecting group) to obtain the cyclopenetanone compound of formula III, (2) methanesulfonylating the product to the mesylate compound of formula IV, (3) treating with a base to effect the first elimination reaction, and (4) treating the resultant compound of formula Vwith an acid to effect the second elimination reaction. |
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EXAMPLE:4-(2-Octenyl)-5-(6-carbonyloxyhexylidene)-cyclopentenone methyl ester. USE:Pharmaceuticals. It has excellent carcinostatic and antiviral activities, and is useful as a carcinostatic agent or a synthetic intermediate of known natural clavulone and claviridenone having strong carcinostatic activity. PREPARATION:The compound of formula I wherein R and R can be prepared by (1) reducing and eliminating the PhSO group of the sulfoxide compound of formula II (R is 1-10C alkyl or ester; R is OH-protecting group) to obtain the cyclopenetanone compound of formula III, (2) methanesulfonylating the product to the mesylate compound of formula IV, (3) treating with a base to effect the first elimination reaction, and (4) treating the resultant compound of formula Vwith an acid to effect the second elimination reaction.</description><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION ORPROCESSING OF GOODS ; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC ; GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS ; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS ; TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINSTCLIMATE CHANGE</subject><creationdate>1986</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19860107&DB=EPODOC&CC=JP&NR=S611636A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76516</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19860107&DB=EPODOC&CC=JP&NR=S611636A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>NOGAMI JIYUNZOU</creatorcontrib><creatorcontrib>KUROZUMI SEIJI</creatorcontrib><title>4-SUBSTITUTED-5-ALKYLIDENE-2-CYCLOPENTENONE AND ITS PREPARATION</title><description>NEW MATERIAL:The compound of formula I (R is 1-10C alkyl, ester, carboxyl, or its salt; R is 1-10C alkyl or alkenyl). EXAMPLE:4-(2-Octenyl)-5-(6-carbonyloxyhexylidene)-cyclopentenone methyl ester. USE:Pharmaceuticals. It has excellent carcinostatic and antiviral activities, and is useful as a carcinostatic agent or a synthetic intermediate of known natural clavulone and claviridenone having strong carcinostatic activity. PREPARATION:The compound of formula I wherein R and R can be prepared by (1) reducing and eliminating the PhSO group of the sulfoxide compound of formula II (R is 1-10C alkyl or ester; R is OH-protecting group) to obtain the cyclopenetanone compound of formula III, (2) methanesulfonylating the product to the mesylate compound of formula IV, (3) treating with a base to effect the first elimination reaction, and (4) treating the resultant compound of formula Vwith an acid to effect the second elimination reaction.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION ORPROCESSING OF GOODS</subject><subject>GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC</subject><subject>GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><subject>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><subject>TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS</subject><subject>TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINSTCLIMATE CHANGE</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1986</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZLA30Q0OdQoO8QwJDXF10TXVdfTxjvTxdHH1c9U10nWOdPbxD3D1C3H18_dzVXD0c1HwDAlWCAhyDXAMcgzx9PfjYWBNS8wpTuWF0twM8m6uIc4euqkF-fGpxQWJyal5qSXxXgHBZoaGZsZmjsaEVQAA7Qwp9A</recordid><startdate>19860107</startdate><enddate>19860107</enddate><creator>NOGAMI JIYUNZOU</creator><creator>KUROZUMI SEIJI</creator><scope>EVB</scope></search><sort><creationdate>19860107</creationdate><title>4-SUBSTITUTED-5-ALKYLIDENE-2-CYCLOPENTENONE AND ITS PREPARATION</title><author>NOGAMI JIYUNZOU ; KUROZUMI SEIJI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JPS611636A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1986</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION ORPROCESSING OF GOODS</topic><topic>GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC</topic><topic>GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><topic>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</topic><topic>TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS</topic><topic>TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINSTCLIMATE CHANGE</topic><toplevel>online_resources</toplevel><creatorcontrib>NOGAMI JIYUNZOU</creatorcontrib><creatorcontrib>KUROZUMI SEIJI</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NOGAMI JIYUNZOU</au><au>KUROZUMI SEIJI</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>4-SUBSTITUTED-5-ALKYLIDENE-2-CYCLOPENTENONE AND ITS PREPARATION</title><date>1986-01-07</date><risdate>1986</risdate><abstract>NEW MATERIAL:The compound of formula I (R is 1-10C alkyl, ester, carboxyl, or its salt; R is 1-10C alkyl or alkenyl). EXAMPLE:4-(2-Octenyl)-5-(6-carbonyloxyhexylidene)-cyclopentenone methyl ester. USE:Pharmaceuticals. It has excellent carcinostatic and antiviral activities, and is useful as a carcinostatic agent or a synthetic intermediate of known natural clavulone and claviridenone having strong carcinostatic activity. PREPARATION:The compound of formula I wherein R and R can be prepared by (1) reducing and eliminating the PhSO group of the sulfoxide compound of formula II (R is 1-10C alkyl or ester; R is OH-protecting group) to obtain the cyclopenetanone compound of formula III, (2) methanesulfonylating the product to the mesylate compound of formula IV, (3) treating with a base to effect the first elimination reaction, and (4) treating the resultant compound of formula Vwith an acid to effect the second elimination reaction.</abstract><oa>free_for_read</oa></addata></record> |
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| subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION ORPROCESSING OF GOODS GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINSTCLIMATE CHANGE |
| title | 4-SUBSTITUTED-5-ALKYLIDENE-2-CYCLOPENTENONE AND ITS PREPARATION |
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