Comprehensive Organic Synthesis II 2014
DOI: 10.1016/b978-0-08-097742-3.00106-3
|View full text |Cite
|
Sign up to set email alerts
|

1.04 Regio-, Diastereo-, and Enantioselective Addition of Organocopper Reagents onto CO and CN Bonds

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2022
2022
2022
2022

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(2 citation statements)
references
References 143 publications
0
2
0
Order By: Relevance
“…Organocopper reagents are widely used in organic synthesis and are routinely obtained by transmetalation reactions of the corresponding organo-magnesium (Grignard reagent), organo-lithium, or organo-zinc precursor by a Cu­(I) salt at low temperature, as depicted in Scheme , eq 1. Those species are known to be thermally unstable and to decompose at low temperature, generally between −90 and 0 °C depending on the nature of the organic moiety.…”
Section: Results and Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Organocopper reagents are widely used in organic synthesis and are routinely obtained by transmetalation reactions of the corresponding organo-magnesium (Grignard reagent), organo-lithium, or organo-zinc precursor by a Cu­(I) salt at low temperature, as depicted in Scheme , eq 1. Those species are known to be thermally unstable and to decompose at low temperature, generally between −90 and 0 °C depending on the nature of the organic moiety.…”
Section: Results and Discussionmentioning
confidence: 99%
“…Organocopper reagents are widely used in organic synthesis and are routinely obtained by transmetalation reactions of the corresponding organo-magnesium (Grignard reagent), organolithium or organo-zinc precursor by a Cu(I) salt at low temperature, [37][38][39][40] as depicted in Scheme 1, eq. 1.…”
Section: State Of the Artmentioning
confidence: 99%