Mild Two-Step Process for the Transition-Metal-Free Synthesis of Carbon−Carbon Bonds from Allylic Alcohols/Ethers and Grignard Reagents
Author:
Affiliation:
1. Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja100747n
Reference41 articles.
1. Asymmetric Transition-Metal-Catalyzed Allylic Alkylations: Applications in Total Synthesis
2. A Concise Account of Recent SN2′ Grignard Coupling Reactions in Organic Synthesis
3. Enantioselective Copper-Catalyzed Conjugate Addition and Allylic Substitution Reactions
4. Copper-catalyzed asymmetric allylic substitution reactions with organozinc and Grignard reagents
5. Nickel-Catalyzed Cross-Couplings of Unactivated Alkyl Halides and Pseudohalides with Organometallic Compounds
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