Total synthesis of (−)-agelastatin A: an S<sub>H</sub>2′ radical azidation strategy

Izuru Tsuchimochi, Yuta Kitamura, Hiroshi Aoyama, Shuji Akai, Keiyo Nakai, Takehiko Yoshimitsu

Chemical Communications · 2018 · 14 citations · 46 references

Concepts

Abstract

2' radical azidation of a bromo silyl enol ether to furnish an azido silyl enol ether via olefin transposition. With the present azidation protocol, a new synthetic approach to agelastatin A, a potent antitumor marine alkaloid, has been established.

References

46