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1. Asymmetric addition of alkenylmetals to aldehydes: Asymmetric addition of alkenylmetals to aldehydes is a chemical reaction in enantioselective synthesis that reacts an alkenylmetal with an aldehyde to give an allyl alcohol (Figure "Asymmetric addition of alkenylmetals to aldehydes"). The stereoselectivity in the reaction is typically controlled ... (Chemistry) [100%] 2023-06-28 [Chemical reactions]
2. Asymmetric addition of dialkylzinc compounds to aldehydes: In asymmetric addition of dialkylzinc compounds to aldehydes dialkyl zinc compounds can be used to perform asymmetric additions to aldehydes, generating substituted alcohols as products (See Barbier reaction). Chiral alcohols are prevalent in many natural products, drugs, and other important ... [92%] 2023-05-09 [Organic reactions]
3. Transition metal complexes of aldehydes and ketones: Transition metal complexes of aldehydes and ketones describes coordination complexes with aldehyde (RCHO) and ketone (R2CO) ligands. Because aldehydes and ketones are common, the area is of fundamental interest. (Chemistry) [92%] 2022-06-15 [Organometallic chemistry] [Transition metals]...
4. Asymmetric addition of alkynylzinc compounds to aldehydes: The asymmetric addition of alkynylzinc compounds to aldehydes is an example of a Nef synthesis, a chemical reaction whereby a chiral propargyl alcohol is prepared from a terminal alkyne and an aldehyde. This alkynylation reaction is enantioselective and involves an ... (Chemistry) [92%] 2023-09-10 [Addition reactions]
5. Asymmetric addition of dialkylzinc compounds to aldehydes: In asymmetric addition of dialkylzinc compounds to aldehydes dialkyl zinc compounds can be used to perform asymmetric additions to aldehydes, generating substituted alcohols as products (See Barbier reaction). Chiral alcohols are prevalent in many natural products, drugs, and other important ... (Chemistry) [92%] 2023-11-15 [Organic reactions]