Diastereoconvergent Negishi Cross-Coupling Using Functionalized Cyclohexylzinc Reagents
Author:
Affiliation:
1. Department Chemie, Ludwig-Maximilian-Universität München, Butenandtstrasse 5-13, 81377, München, Germany
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol403673e
Reference60 articles.
1. Secondary Alkyl Halides in Transition-Metal-Catalyzed Cross-Coupling Reactions
2. Advances in Transition Metal (Pd,Ni,Fe)-Catalyzed Cross-Coupling Reactions Using Alkyl-organometallics as Reaction Partners
3. Transition Metal-Catalyzed Direct Arylation of Substrates with Activated sp3-Hybridized C−H Bonds and Some of Their Synthetic Equivalents with Aryl Halides and Pseudohalides
4. Cross-Coupling of C(sp3)-H Bonds with Organometallic Reagents via Pd(II)/Pd(0) Catalysis
5. Highly diastereoselective Csp3–Csp2 Negishi cross-coupling with 1,2-, 1,3- and 1,4-substituted cycloalkylzinc compounds
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