Natural Products Chemistry, Band 3Koji Nakanishi, Kōji Nakanishi Kodansha, 1974 - 700 Seiten |
Inhalt
Mono and Sesquiterpenoids | 9 |
Di and Higher Terpenoids | 105 |
Steroids | 176 |
Urheberrecht | |
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Häufige Begriffe und Wortgruppen
¹³C-nmr absolute configuration Ac₂0/py Acad acetate acid AcOH Acta aldehyde alkaloids Antibiot bacteriorhodopsin Batrachotoxin Biochem Biophys biosynthesis carbon CH₂ CH₂OH Chem chemical Chemistry Chim chiral chromophore CO₂Me Commun compound COOCH3 COOEt COOH COOME cyclization derivative diastereomers double bond E.J. Corey epimer epoxide ester EtOH H COOH H H H H OH H-nmr H₂ HMPA HOOC humulene hydrogen hydrolysis hydroxyl ibid intermediate isolated isomer isomerization Jones oxidation ketone lactone Lett leukotriene LiAlH mCPBA MeOH MeOOC methyl methyl group mixture moiety NaBH NaBH4 Nakanishi NaOH OCH₂Ph OCH3 OH H OH OH OH OMe OMe opsin OTHP p-TSOH Phytochemistry proton R₁ R₂ reaction reagent rearrangement reduction Remarks rhodopsin ring Route sesquiterpenes skeleton stereochemistry stereoselective steroid Structure and Synthesis Tetr Tetrahedron total synthesis TsCl/py TSOH x-ray analysis yield ОН ОН