Synthesen in der Carotinoid‐Reihe. 8. Mitteilung. Totalsynthese von Kryptoxanthin und eine weitere Synthese von Zeaxanthin
Cryptoxanthin has been synthesized from acetoxy‐β‐C19‐aldehyde and β‐C21‐acetylenic carbinol following the scheme C19 + C21 = C40. The C19‐aldehyde was obtained from keto‐iso‐C14‐aldehyde via the acetoxy‐β‐C14‐ and ‐C14‐aldehydes. The optically inactive synthetic cryptoxanthin has the same melting p...
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Veröffentlicht in: | Helvetica chimica acta 1957, Vol.40 (2), p.456-467 |
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creator | Isler, O. Lindlar, H. Montavon, M. Rüegg, R. Saucy, G. Zeller, P. |
description | Cryptoxanthin has been synthesized from acetoxy‐β‐C19‐aldehyde and β‐C21‐acetylenic carbinol following the scheme C19 + C21 = C40. The C19‐aldehyde was obtained from keto‐iso‐C14‐aldehyde via the acetoxy‐β‐C14‐ and ‐C14‐aldehydes. The optically inactive synthetic cryptoxanthin has the same melting point as the natural product, and the absorption spectra of the solutions are identical. Starting with the acetoxy‐β‐C19‐aldehyde, an improved synthesis of zeaxanthin was developped, following the scheme C19 + C2 + C19. |
doi_str_mv | 10.1002/hlca.19570400225 |
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Totalsynthese von Kryptoxanthin und eine weitere Synthese von Zeaxanthin</title><source>Access via Wiley Online Library</source><creator>Isler, O. ; Lindlar, H. ; Montavon, M. ; Rüegg, R. ; Saucy, G. ; Zeller, P.</creator><creatorcontrib>Isler, O. ; Lindlar, H. ; Montavon, M. ; Rüegg, R. ; Saucy, G. ; Zeller, P.</creatorcontrib><description>Cryptoxanthin has been synthesized from acetoxy‐β‐C19‐aldehyde and β‐C21‐acetylenic carbinol following the scheme C19 + C21 = C40. The C19‐aldehyde was obtained from keto‐iso‐C14‐aldehyde via the acetoxy‐β‐C14‐ and ‐C14‐aldehydes. The optically inactive synthetic cryptoxanthin has the same melting point as the natural product, and the absorption spectra of the solutions are identical. Starting with the acetoxy‐β‐C19‐aldehyde, an improved synthesis of zeaxanthin was developped, following the scheme C19 + C2 + C19.</description><identifier>ISSN: 0018-019X</identifier><identifier>EISSN: 1522-2675</identifier><identifier>DOI: 10.1002/hlca.19570400225</identifier><language>eng</language><publisher>Weinheim: WILEY‐VCH Verlag GmbH</publisher><ispartof>Helvetica chimica acta, 1957, Vol.40 (2), p.456-467</ispartof><rights>Copyright © 1957 Verlag GmbH & Co. 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Mitteilung. Totalsynthese von Kryptoxanthin und eine weitere Synthese von Zeaxanthin</title><title>Helvetica chimica acta</title><description>Cryptoxanthin has been synthesized from acetoxy‐β‐C19‐aldehyde and β‐C21‐acetylenic carbinol following the scheme C19 + C21 = C40. The C19‐aldehyde was obtained from keto‐iso‐C14‐aldehyde via the acetoxy‐β‐C14‐ and ‐C14‐aldehydes. The optically inactive synthetic cryptoxanthin has the same melting point as the natural product, and the absorption spectra of the solutions are identical. Starting with the acetoxy‐β‐C19‐aldehyde, an improved synthesis of zeaxanthin was developped, following the scheme C19 + C2 + C19.</description><issn>0018-019X</issn><issn>1522-2675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1957</creationdate><recordtype>article</recordtype><recordid>eNqFkLFOwzAURS0EEqWwM_oHEp6d2okHhioCighCokVCLJGTPlOj4FROSonEwCfwjXwJqdqhG9PTfTrnDpeQcwYhA-AXi6rUIVMihlEfuTggAyY4D7iMxSEZALAkAKaej8lJ07wBgFIQD8jXtHPtAht01Do6R09T7evWutrOf79_HtEuMKRJSO9t26KtVu41pLO61VWzE-lH7eid75Zt_an7V1-zcnOK1iFdo23RI53usy-od-ApOTJ9EZ7t7pA8XV_N0kmQPdzcpuMsKDkkIpBKCgkKtExMWRqOkiMkhYmENEpFOIohSuLCSIZQmIIVwHWcSK241przOBoS2PaWvm4ajyZfevuufZczyDfr5Zv18r31euVyq6xthd2_fD7J0vG-_wcyungu</recordid><startdate>1957</startdate><enddate>1957</enddate><creator>Isler, O.</creator><creator>Lindlar, H.</creator><creator>Montavon, M.</creator><creator>Rüegg, R.</creator><creator>Saucy, G.</creator><creator>Zeller, P.</creator><general>WILEY‐VCH Verlag GmbH</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>1957</creationdate><title>Synthesen in der Carotinoid‐Reihe. 8. 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Totalsynthese von Kryptoxanthin und eine weitere Synthese von Zeaxanthin</title><author>Isler, O. ; Lindlar, H. ; Montavon, M. ; Rüegg, R. ; Saucy, G. ; Zeller, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2085-69656090a68fccf2e62e08bf356f993e470387bf61e0bfb1b02a786a92aaa2273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1957</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Isler, O.</creatorcontrib><creatorcontrib>Lindlar, H.</creatorcontrib><creatorcontrib>Montavon, M.</creatorcontrib><creatorcontrib>Rüegg, R.</creatorcontrib><creatorcontrib>Saucy, G.</creatorcontrib><creatorcontrib>Zeller, P.</creatorcontrib><collection>CrossRef</collection><jtitle>Helvetica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Isler, O.</au><au>Lindlar, H.</au><au>Montavon, M.</au><au>Rüegg, R.</au><au>Saucy, G.</au><au>Zeller, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesen in der Carotinoid‐Reihe. 8. Mitteilung. Totalsynthese von Kryptoxanthin und eine weitere Synthese von Zeaxanthin</atitle><jtitle>Helvetica chimica acta</jtitle><date>1957</date><risdate>1957</risdate><volume>40</volume><issue>2</issue><spage>456</spage><epage>467</epage><pages>456-467</pages><issn>0018-019X</issn><eissn>1522-2675</eissn><abstract>Cryptoxanthin has been synthesized from acetoxy‐β‐C19‐aldehyde and β‐C21‐acetylenic carbinol following the scheme C19 + C21 = C40. The C19‐aldehyde was obtained from keto‐iso‐C14‐aldehyde via the acetoxy‐β‐C14‐ and ‐C14‐aldehydes. The optically inactive synthetic cryptoxanthin has the same melting point as the natural product, and the absorption spectra of the solutions are identical. Starting with the acetoxy‐β‐C19‐aldehyde, an improved synthesis of zeaxanthin was developped, following the scheme C19 + C2 + C19.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH</pub><doi>10.1002/hlca.19570400225</doi><tpages>12</tpages></addata></record> |
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title | Synthesen in der Carotinoid‐Reihe. 8. Mitteilung. Totalsynthese von Kryptoxanthin und eine weitere Synthese von Zeaxanthin |
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