Shun Hirasawa, Tsuyoshi Masuda, Ken Mukai, Yusuke Miyoshi and Nobuhiro Kanomata
Org. Biomol. Chem., 2021,19, 6897-6903
DOI:
10.1039/D1OB00952D,
Paper
We herein report a novel, short asymmetric synthesis of (−)-dehydro-exo-brevicomin (DHB, 1), a sex pheromone isolated from house mice, in 44% overall yield, the highest yield reported so far, over eight steps from trans-3-hexen-1-ol (7). We successfully prepared the target molecule (−)-1 from spontaneous intramolecular acetalisation after the photoisomerisation of trans-enone 6, which generated the corresponding cis-enone 5in situ, the possible biosynthetic precursor of DHB.