Reactions of 5,6-Dilithioacenaphthene-N,N,N′,N′-Tetramethyl-1,2-ethanediamine Complex with α-Diketones. I.cis-Directing 1:1 Cyclic Additions with Acyclic and Cyclic α-Diketones and Related Compounds
نویسندگان
چکیده
منابع مشابه
Thiazolium-catalyzed intermolecular Stetter reaction of linear and cyclic alkyl α-diketones.
An efficient method for the N-heterocyclic carbene (NHC)-catalyzed conjugate addition of acetyl anions to various α,β-unsaturated acceptors (Stetter reaction) has been optimized by using 2,3-butandione (biacetyl) as an alternative surrogate of acetaldehyde. The disclosed procedure proved to be compatible with microwave dielectric heating for reaction time reduction and with the use of different...
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The 1,4-conjugate addition of nucleophiles to α,β-unsaturated carbonyl compounds represents one fundamental bond-forming reaction in organic synthesis. The development of effective organocatalysts for the enantioselective conjugate addition of malonate, nitroalkane and other carbon and heteroatom nucleophiles to cycloenones constitutes an important research field and has been explored in recent...
متن کاملThe asymmetric synthesis of chiral cyclic α-hydroxy phosphonates and quaternary cyclic α-hydroxy phosphonates.
A highly practical, catalytic enantioselective cyclic phosphite addition to aldehydes and ketones was developed. The reaction rate of the asymmetric hydrophosphonylation was significantly enhanced by the addition of silver carbonate. Particularly, significant improvement has been achieved on the asymmetric hydrophosphonylation of unactivated ketones, giving quaternary α-hydroxy phosphonates wit...
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ژورنال
عنوان ژورنال: Bulletin of the Chemical Society of Japan
سال: 1981
ISSN: 0009-2673,1348-0634
DOI: 10.1246/bcsj.54.3020