File:Enantioselective Ir-Catalyzed Bidirectional Reductive Coupling (MédiHAL 1987324).jpg
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Summary
[edit]DescriptionEnantioselective Ir-Catalyzed Bidirectional Reductive Coupling (MédiHAL 1987324).jpg |
English: In the presence of a chiral iridium complex, commercially available 3-chloro-2-chloromethyl-1-propene (1) was selectively activated for various reductive couplings. Depending on the reaction conditions it allows a selective mono- or bidirectional condensation with one or two external aldehydes with excellent enantiocontrol (>90% ee). This approach occurring simply under mild conditions and avoiding premetalated reagents constructs rapidly chiral homoallylic alcohols, key precursors of important molecular fragments such as furans, pyrans, ketodiols, or 1,3,5-polyols. |
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Date | Taken on 8 January 2019 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Source | Enantioselective Ir-Catalyzed Bidirectional Reductive Coupling | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Author |
Adrien Quintard, Jean Rodriguez
creator QS:P170,Q81717626
institution QS:P195,Q30295259
institution QS:P195,Q2302586
institution QS:P195,Q3152386
institution QS:P195,Q280413 |
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Keywords InfoField | Reductive coupling; Catalysis; Iridium; Enantioselective synthesis |
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[edit]Public domainPublic domainfalsefalse |
This work is in the public domain in France for one of the following reasons:
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Short title | Enantioselective Ir-Catalyzed Bidirectional Reductive Coupling |
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Headline | Enantioselective Ir-Catalyzed Bidirectional Reductive Coupling |
Author |
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Image title | In the presence of a chiral iridium complex, commercially available 3-chloro-2-chloromethyl-1-propene (1) was selectively activated for various reductive couplings. Depending on the reaction conditions it allows a selective mono- or bidirectional condensation with one or two external aldehydes with excellent enantiocontrol (>90% ee). This approach occurring simply under mild conditions and avoiding premetalated reagents constructs rapidly chiral homoallylic alcohols, key precursors of important molecular fragments such as furans, pyrans, ketodiols, or 1,3,5-polyols. |
JPEG file comment | CREATOR: gd-jpeg v1.0 (using IJG JPEG v62), quality = 75 |
Keywords |
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Code for country shown | FR |
Country shown | France |