N-Heterocyclic Carbene-Catalyzed Atroposelective Synthesis of N-N Axially Chiral 3-Amino Quinazolinones

被引:37
作者
Balanna, Kuruva [1 ]
Barik, Soumen [1 ]
Barik, Shilpa [1 ]
Shee, Sayan [1 ]
Manoj, Niket [1 ]
Gonnade, Rajesh G. [2 ]
Biju, Akkattu T. [1 ]
机构
[1] Indian Inst Sci, Dept Organ Chem, Bangalore 560012, India
[2] Ctr Mat Characterizat, CSIR, Natl Chem Lab, Pune 411008, India
关键词
organocatalysis; N-heterocycliccarbenes; asymmetriccatalysis; axial chirality; amino quinazolinones; KINETIC RESOLUTION; ACYL; DESYMMETRIZATION; CONSTRUCTION; ATROPISOMERS; MECHANISM; ACCESS;
D O I
10.1021/acscatal.3c01709
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Although the atroposelective synthesisof biaryls and related compoundsbearing axially chiral C-C bonds is well-known, the synthesisof axially chiral C-N bond-containing compounds is relativelyless explored, and the construction of axially chiral N-N bondshas received only scant attention. Demonstrated herein is the N-heterocycliccarbene (NHC)-catalyzed selective amidation reaction, leading to theatroposelective synthesis of N-N axially chiral 3-amino quinazolinones.The NHC-catalyzed reaction of quinazolinones containing a free N-Hmoiety with & alpha;,& beta;-unsaturated aldehydes under oxidativeconditions furnished the atropisomeric quinazolinone derivatives undermild conditions and broad scope. Preliminary studies on experimentaland density functional theory-based N-N rotational barrierdetermination are also presented.
引用
收藏
页码:8752 / 8759
页数:8
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