2010
DOI: 10.1002/chin.201016086
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: A Direct Approach to 5‐Hydroxybenzofurans via a Platinum‐Catalyzed Domino Rearrangement/5‐endo‐dig Cyclization Reaction of Quinols.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2022
2022
2022
2022

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 1 publication
0
1
0
Order By: Relevance
“…25 In 2009, Kim's group developed a direct and efficient approach to access 5-hydroxybenzofurans 47 under platinum catalysis (Scheme 18). 26 Enynols 46 bearing both aryl and alkyl groups were compatible with this protocol, and a series of 5-hydroxybenzofurans 47 were successfully formed in moderate to excellent yields under mild conditions. This novel transformation proceeded via a platinum-catalyzed cascade dienone-phenol rearrangement/5endo-dig cyclization sequence to afford the target products.…”
Section: Qiang Xiaomentioning
confidence: 95%
“…25 In 2009, Kim's group developed a direct and efficient approach to access 5-hydroxybenzofurans 47 under platinum catalysis (Scheme 18). 26 Enynols 46 bearing both aryl and alkyl groups were compatible with this protocol, and a series of 5-hydroxybenzofurans 47 were successfully formed in moderate to excellent yields under mild conditions. This novel transformation proceeded via a platinum-catalyzed cascade dienone-phenol rearrangement/5endo-dig cyclization sequence to afford the target products.…”
Section: Qiang Xiaomentioning
confidence: 95%