Asymmetric Total Synthesis of (−)-Spirochensilide A, Part 1: Diastereoselective Synthesis of the ABCD Ring and Stereoselective Total Synthesis of 13(R)-Demethyl Spirochensilide A

Author:

Liang Xin-Ting1,Sun Bao-Chuan1,Liu Chang1,Li Yuan-He1,Zhang Nan1,Xu Qian-Qian1,Zhang Zhong-Chao2ORCID,Han Yi-Xin1,Chen Jia-Hua1,Yang Zhen123ORCID

Affiliation:

1. State Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education and Beijing National Laboratory for Molecular Science (BNLMS), College of Chemistry, Peking University, Beijing 100871, China

2. Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen 518055, China

3. Shenzhen Bay Laboratory, Shenzhen 518055, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Reference110 articles.

1. Phytochemical and Biological Studies ofAbies Species

2. Zheng, W. J.; Fu, L. G. Flora of China; Wu, Z. Y., Ed. Science Press: Beijing, 1978; Vol. 7, p 68.

3. Huang, L. Q.; Hao, J. D.; Shao, A. J. National compilation of Chinese herbal medicine, 3rd ed.; Wang, G. Q., Ed. People’s Medical Publishing House Co., Ltd.: Beijing, 2014; Vol. 3, p 463.

4. Spirochensilides A and B, Two New Rearranged Triterpenoids from Abies chensiensis

5. Therapeutic potential of inhibition of the NF-κB pathway in the treatment of inflammation and cancer

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