Categories: Synthesis of N-Heterocycles > benzo-fused N-Heterocycles >
Synthesis of tetrahydroquinazolines
Recent Literature
An iridium-catalyzed asymmetric [4 + 2] cycloaddition of 1,3,5-triazinanes
with 2-(1-hydroxyallyl)anilines/2-(1-hydroxyallyl)phenols provides a wide range
of tetrahydroquinazolines in good yields and excellent enantioselectivities. In
addition, chiral 1,3-benzoxazines, which are challenging products, could also be
obtained in excellent enantioselectivities using this protocol.
S. Tang, Z. Cheng, P. Zhang, Y. Shao, J. Sun, Org. Lett., 2023, 25,
3639-3643.
A copper-catalyzed asymmetric formal [4 + 2]-cycloaddition of
copper-allenylidenes and hexahydro-1,3,5-triazines provides chiral
tetrahydroquinazolines in good yields and with high enantioselectivities for
most cases.
D. Ji, C. Wang, J. Sun, Org. Lett.,
2018, 20, 3710-3713.