TY - JOUR
AU - Maruoka, Keiji
AB - A synthesis of acyl halides from the corresponding carboxylic acid thioesters was achieved using commercially available Selectfluor or NCS, and the acyl fluoride or chloride intermediates were transformed to the corresponding esters, amides, and several carbon‐carbon bond formation products. This approach can be applied to the peptide synthesis from functionalized amino acid thioesters.
TI - Synthesis of Acyl Halides from Carboxylic Acid Thioesters for Synthesis of Ketones, Esters, Amides and Peptides
JF - Advanced Synthesis & Catalysis
DO - 10.1002/adsc.202400531
DA - 2024-10-08
UR - https://www.deepdyve.com/lp/wiley/synthesis-of-acyl-halides-from-carboxylic-acid-thioesters-for-kL2BgiwU3e
SP - 4061
EP - 4065
VL - 366
IS - 19
DP - DeepDyve
ER -