Recent advances in abietane/icetexane synthesis
- Authors
- Kang, Juyeon; Quynh Le, Thuy; Oh, Chang Ho
- Issue Date
- Oct-2022
- Publisher
- Elsevier BV
- Keywords
- Diterpenoid; Abietane; Icetexane; Synthetic strategies
- Citation
- Tetrahedron Letters, v.108, no.SI, pp 1 - 28
- Pages
- 28
- Indexed
- SCIE
SCOPUS
- Journal Title
- Tetrahedron Letters
- Volume
- 108
- Number
- SI
- Start Page
- 1
- End Page
- 28
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/190532
- DOI
- 10.1016/j.tetlet.2022.154133
- ISSN
- 0040-4039
1873-3581
- Abstract
- Developed synthetic strategies for abietane and icetexane diterpenoids during 2010-present are described in this review. To date, the [6–6–6]- and [6–7–6]-tricyclic skeletons of diterpenoids have been constructed by applying enzymatic synthesis, chemical synthesis, and semisynthesis. The ring expansion approach in semisynthesis has the advantage of generating a flexible skeleton of icetexane diterpenoid from abietane diterpenoid. Continuous research on the synthetic strategies of these diterpenoids is important for the development of new pharmaceutical and chemical industries.
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