Synthetic Study on Lactonamycins, Part 2: Stereoselective Access to ABCD-Ring System.

Autor: Takikawa, Hiroshi, Murata, Kazuki, Sato, Shogo, Kawada, Takuma, Nakakohara, Hiroshi, Ohmori, Ken, Suzuki, Keisuke
Předmět:
Zdroj: Synlett; 2020, Vol. 31 Issue 16, p1623-1628, 6p
Abstrakt: Toward a stereoselective total synthesis of the lactonamycins, we recently reported an approach to the DEF-ring system. Here we report a model study for constructing the ABCD-ring system, revealing a viable approach through (1) construction of the C-ring by asymmetric benzoin cyclization, (2) introduction of an angular hydroxy group through oxidation of an isoxazolium salt, and (3) construction of the AB rings through a ring-opening/closing sequence. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index