A Synthetic Approach to (±)Pumiliotoxin C via retro-Michael Reaction

  • KYOOHYUN CHUNG

초록

A stereoselective synthesis of methyl 2-amino-6-methylcyclohexane carboxylate, a key intermediate, was achieved by a base induced rearrangement of 7-oxabicyclo[2.2.1]heptane followed by the conjugate addition fo the resulting conjugated ester with Me2LiCu.

제목
A Synthetic Approach to (±)Pumiliotoxin C via retro-Michael Reaction
저자
KYOOHYUN CHUNG
학회명
대한화학회 제88회 총회 및 학술발표회 진행표 및 논문초록