Abstract
A facile and efficient total synthesis of bioactive sansalvamide A peptide has been accomplished, including the‐ionic‐liquid supported method and final PyBOP‐promoted ring closure.
Acknowledgments
We gratefully acknowledge generous support from the National Natural Science Foundation of China (Grants 20372069, 29725203, and 20472094), the Key Technologies R&D Program from CAS (Grants 2005BA711A01), and the 863 Hi‐Tech Program of China (Grants 2006AA020402 and 2006AA020602).