Stereoselective Synthesis of the CDE Ring System of Antitumor Saponin Scillascilloside E-1
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-dori, Mizuho-ku, Nagoya 467-8603, Japan
2. Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol500657f
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2. Eucosterol Oligoglycosides Isolated from Scilla scilloides and Their Anti-tumor Activity.
3. First demonstration of a carbocation-olefin cyclization route to the lanosterol series
4. Total synthesis of fomitellic acid B
5. Synthesis of Chiral Building Blocks for Oxygenated Terpenoids through a Simultaneous and Stereocontrolled Construction of Contiguous Quaternary Stereocenters by an Ireland–Claisen Rearrangement
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