Asymmetric diels-alder cycloaddition with chiral 2-alkylsulfinyl-1-nitroalkenes

Kaoru Fuji; Kiyoshi Tanaka; Hitoshi Abe; Akichika Itoh; Manabu Node; Tooru Taga; Yoshihisa Miwa; Motoo Shiro

doi:10.1016/S0957-4166(00)82353-8

Asymmetric diels-alder cycloaddition with chiral 2-alkylsulfinyl-1-nitroalkenes

Kaoru Fuji^*, Kiyoshi Tanaka, Hitoshi Abe, Akichika Itoh, Manabu Node, Tooru Taga, Yoshihisa Miwa, Motoo Shiro

^*この論文の責任著者

工学科　応用化学コース

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

22 被引用数 (Scopus)

抄録

The Diels-Alder reaction of chiral 2-alkylsulfinyl-1-nitroalkene 1 and Danishefsky's diene (2) afforded adducts 3 and 4 in good chemical yield with a high enantiomeric excess, while diastereomeric nitroalkene 7 gave 8 and 9, enantiomeric to 3 and 4, respectively,.

本文言語	英語
ページ（範囲）	179-182
ページ数	4
ジャーナル	Tetrahedron Asymmetry
巻	2
号	3
DOI	https://doi.org/10.1016/S0957-4166(00)82353-8
出版ステータス	出版済み - 1991

ASJC Scopus 主題領域

触媒
物理化学および理論化学
有機化学
無機化学

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10.1016/S0957-4166(00)82353-8

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@article{146a2cfd95a6479d8a6281a2ce64fb45,

title = "Asymmetric diels-alder cycloaddition with chiral 2-alkylsulfinyl-1-nitroalkenes",

abstract = "The Diels-Alder reaction of chiral 2-alkylsulfinyl-1-nitroalkene 1 and Danishefsky's diene (2) afforded adducts 3 and 4 in good chemical yield with a high enantiomeric excess, while diastereomeric nitroalkene 7 gave 8 and 9, enantiomeric to 3 and 4, respectively,.",

author = "Kaoru Fuji and Kiyoshi Tanaka and Hitoshi Abe and Akichika Itoh and Manabu Node and Tooru Taga and Yoshihisa Miwa and Motoo Shiro",

year = "1991",

doi = "10.1016/S0957-4166(00)82353-8",

language = "英語",

volume = "2",

pages = "179--182",

journal = "Tetrahedron Asymmetry",

issn = "0957-4166",

publisher = "Elsevier Ltd.",

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TY - JOUR

T1 - Asymmetric diels-alder cycloaddition with chiral 2-alkylsulfinyl-1-nitroalkenes

AU - Fuji, Kaoru

AU - Tanaka, Kiyoshi

AU - Abe, Hitoshi

AU - Itoh, Akichika

AU - Node, Manabu

AU - Taga, Tooru

AU - Miwa, Yoshihisa

AU - Shiro, Motoo

PY - 1991

Y1 - 1991

N2 - The Diels-Alder reaction of chiral 2-alkylsulfinyl-1-nitroalkene 1 and Danishefsky's diene (2) afforded adducts 3 and 4 in good chemical yield with a high enantiomeric excess, while diastereomeric nitroalkene 7 gave 8 and 9, enantiomeric to 3 and 4, respectively,.

AB - The Diels-Alder reaction of chiral 2-alkylsulfinyl-1-nitroalkene 1 and Danishefsky's diene (2) afforded adducts 3 and 4 in good chemical yield with a high enantiomeric excess, while diastereomeric nitroalkene 7 gave 8 and 9, enantiomeric to 3 and 4, respectively,.

UR - http://www.scopus.com/inward/record.url?scp=0025809856&partnerID=8YFLogxK

U2 - 10.1016/S0957-4166(00)82353-8

DO - 10.1016/S0957-4166(00)82353-8

M3 - 学術論文

AN - SCOPUS:0025809856

SN - 0957-4166

VL - 2

SP - 179

EP - 182

JO - Tetrahedron Asymmetry

JF - Tetrahedron Asymmetry

IS - 3

ER -

Asymmetric diels-alder cycloaddition with chiral 2-alkylsulfinyl-1-nitroalkenes

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