The selective conversion of alkenes into alcohols is a cornerstone of modern chemical synthesis, underpinning the production ...
Researchers at the Max-Planck-Institut für Kohlenforschung have unveiled a two-step alkene alkylation method using stable carboxylic acids and polar coupling. The approach overcomes a long-standing ...
Chemists at the Max-Planck-Institut für Kohlenforschung have developed a practical two-step method for alkylating alkenes via thianthrenation, addressing a long-standing synthetic challenge. This ...
A line structure of a molecule derived from the natural product 3-carene; the parent 3-carene structure, featuring a six-carbon ring with a double bond, is in blue and the added portion, featuring a ...
† Beijing National Laboratory of Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing ...
Carbonyls and alkenes, two of the most common functional groups in organic chemistry, generally do not react with one another. Now, a simple Lewis acid has been shown to catalyse metathesis between ...
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