Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sheng-Mou Hu"'
Publikováno v:
Tetrahedron Letters. 81:153363
Orthoesters based on phragmalin-type limonoid from Meliaceae family is an important branch of plant orthoesters, and it is mainly existed as 1/8/9-, 8/9/11-, 8/9/14-, or 8/9/30-types. In the process of exploring the biogenetic pathway of the orthoest
Autor:
Wansha Huang, Can Zhang, Sheng-Mou Hu, Xiao-Bing Wang, Chen Wang, Ling-Yi Kong, Ming-Hua Yang, Yi-Jun Chen, Hequan Yao, Jian-Guang Luo, Xu-Wei Zhou, Panpan Zhang, Hongbin Sun, Chang Liu, Jun Luo
Publikováno v:
Organic Chemistry Frontiers. 4:2417-2421
Tooniliatone A (1), a novel limonoid with an unprecedented 6/5/6/5 tetracarbocyclic skeleton was isolated from Toona ciliata Roem. var. yunnanensis. Its rearranged ring-seco backbone was proposed to biosynthetically originate from co-isolated known t
Publikováno v:
Tetrahedron. 71:8472-8477
Eight new compounds, including four rare B-seco-29-nor-limonoids, toonaciliatones A-D (1–4), and four normal B-seco-limonoids, toonaciliatones E-H (5–8), together with six known compounds (9–14), were isolated from the stem barks of Toona cilia
Publikováno v:
Phytomedicine. 62:152947
Background Multidrug resistance (MDR) refers to the phenotype of tumor cells that are resistant to various chemotherapeutic drugs with different structures and functions, which is clearly disadvantageous for patients. Finding a natural product that c
Publikováno v:
ChemInform. 47
Eight new compounds, including four rare B-seco-29-nor-limonoids, toonaciliatones A-D (1–4), and four normal B-seco-limonoids, toonaciliatones E-H (5–8), together with six known compounds (9–14), were isolated from the stem barks of Toona cilia
Publikováno v:
Tetrahedron Letters. 55:815-817
The orthoester, a functional group that features three alkoxy groups attaching to a single carbon atom, was an important structural subunit discovered in plant resource. Diverse phragmalin-type limonoids with different orthoester moiety and connected
Publikováno v:
ChemInform. 45
An efficient and concise method for the preparation of compounds (I) from tabulalin is reported.