“…In this work, the cyclization reaction of propargylic amides 28–31 was investigated using Ph 3 PAuCl as a catalyst and halogen bond donors (C 4 H 2 INO 2 , C 6 F 5 I, C 8 H 9 O 2 I) as activators. We mainly focused on the following points: (1) designing and assessing two activation modes in gold( i ) catalysis: the halogen bond donor activates the Cl atom of Ph 3 PAuCl to form X–I⋯Cl (X = C, N) classical halogen bonding and activates the Au atom of Ph 3 PAuCl to form X–I⋯Au (X = C, N) metal-involved halogen bonding; (2) investigating the reaction mechanism of the cyclization reaction of propargylic amides by using halogen bond activation to gold( i ) catalysts; (3) comparing the activation ability of metal-involved halogen bonding and classical halogen bonding for gold( i ) catalysts.…”
In gold(I) catalysis, the activation of Au(I) chloride catalysts by chloride abstraction by noncovalent interactions has become a research focus of organometallic catalysis. In this work, taking halogen bond donors...
“…In this work, the cyclization reaction of propargylic amides 28–31 was investigated using Ph 3 PAuCl as a catalyst and halogen bond donors (C 4 H 2 INO 2 , C 6 F 5 I, C 8 H 9 O 2 I) as activators. We mainly focused on the following points: (1) designing and assessing two activation modes in gold( i ) catalysis: the halogen bond donor activates the Cl atom of Ph 3 PAuCl to form X–I⋯Cl (X = C, N) classical halogen bonding and activates the Au atom of Ph 3 PAuCl to form X–I⋯Au (X = C, N) metal-involved halogen bonding; (2) investigating the reaction mechanism of the cyclization reaction of propargylic amides by using halogen bond activation to gold( i ) catalysts; (3) comparing the activation ability of metal-involved halogen bonding and classical halogen bonding for gold( i ) catalysts.…”
In gold(I) catalysis, the activation of Au(I) chloride catalysts by chloride abstraction by noncovalent interactions has become a research focus of organometallic catalysis. In this work, taking halogen bond donors...
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