Development of Synthetic Methodologies for Heterocycles Using Diene-transmissive Hetero-Diels-Alder Reaction

被引:0
|
作者
Saito, Takao [1 ]
Kobayashi, Satoru [2 ]
Otani, Takashi [3 ]
Kutsumura, Noriki [4 ]
机构
[1] Tokyo Univ Sci, Fac Sci, Dept Chem, Shinjuku Ku, Tokyo 1628601, Japan
[2] Japan Tabacco Inc, Cent Pharmaceut Res Inst, 1-1 Murasaki Cho, Takatsuki, Osaka 5691125, Japan
[3] Anan Coll, Natl Inst Technol, Course Chem Engn, 265 Aoki, Minobaya, Anan 7740017, Japan
[4] Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan
关键词
heterocycles; DTHDA reaction; azatriene; thiatriene; oxatriene; dioxatriene; dendralene; Diels-Alder reaction; tandem reaction; CROSS-CONJUGATED TRIENES; STEREO-CONTROLLED SYNTHESIS; VERSATILE BUILDING-BLOCKS; STEREOSELECTIVE-SYNTHESIS; ENANTIOSELECTIVE SYNTHESIS; CYCLOADDITION REACTION; POLYCYCLIC COMPOUNDS; ORGANIC-SYNTHESIS; AZATRIENES; EFFICIENT;
D O I
10.5059/yukigoseikyokaishi.74.803
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The diene-transmissive hetero-Diels-Alder reaction (DTHDA reaction) is a special case of the DTDA reaction in which one or more heteroatoms are contained within either a cross-conjugated triene/polyene (heterodendralene) pi-system, a dienophile pi-system or both. Therefore, the DTHDA protocol is an efficient and attractive method for the stereoselective synthesis of a variety of heterocyclic systems. Merits and potential of the DTHDA methodology for heterocyclic synthesis can be widely extended by structural variations and complexity of both diene and dienophile; the kind, numbers, and positions of heteroatoms contained in either the cross-conjugated triene/polyene ( [3/n] heterodendralene) or the dienophile framework, as well as the inter or intramolecular cycloaddition mode, and its predictable regio- and stereoselectivities. In this paper, we introduce the synthesis of a variety of heterocycles using the DTHDA reaction with a focus on our research.
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页码:803 / 813
页数:11
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