An asymmetric synthesis of (+)-Scrodentoid A from dehydroabietic acid

An efficient synthesis of (+)-scrodentoid A was accomplished starting from commercially available dehydroabietic acid. Key reactions in the synthesis include oxidative decarboxylation of dehydroabietic acid and C–H bond oxidation on arene. To create your abstract, type over the instructions in the t...

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Bibliographic Details
Published inTetrahedron Vol. 85; pp. 132031 - 132035
Main Authors Song, Yi-Kang, Liu, Li, Wang, Jun-Jie, Qian, Fei, Yang, Mao-Qi, Zhang, Liu-Qiang, Fu, Jian-Guo, Li, Yi-Ming, Feng, Chen-Guo
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 09.04.2021
Elsevier
Subjects
(+)-Scrodentoid A
Chemistry
Chemistry, Organic
C–H Bond oxidation
Oxidative decarboxylation
Physical Sciences
Science & Technology
Synthesis
(+)-Scrodentoid A
C–H Bond oxidation
Synthesis
Oxidative decarboxylation
AROMATIC ABIETANE DITERPENOIDS
OXIDATION
BIOLOGICAL-ACTIVITY
C-H Bond oxidation
CARBONYL-COMPOUNDS
METHYLENATION
DERIVATIVES
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Summary:An efficient synthesis of (+)-scrodentoid A was accomplished starting from commercially available dehydroabietic acid. Key reactions in the synthesis include oxidative decarboxylation of dehydroabietic acid and C–H bond oxidation on arene. To create your abstract, type over the instructions in the template box below. Fonts or abstract dimensions should not be changed or altered. Leave this area blank for abstract info. [Display omitted]
ISSN:0040-4020
1464-5416
DOI:10.1016/j.tet.2021.132031