We have studied the remarkable dependence of the stereochemistry of the cyclization on the double bond geometry and of the effect of the bulkiness of the nucleophile on the regiochemistry of the palladium mediated cyclization of alkenes bearing aryl bromides and nucleophiles. In contrast. the cyclization of the acetylenic homologous substrates is not dependent on the nature of the nucleophile. (C) 2004 Elsevier Ltd. All rights reserved.
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Kyoto Inst Technol, Dept Chem & Mat Technol, Sakyo Ku, Kyoto 6060962, JapanKyoto Inst Technol, Dept Chem & Mat Technol, Sakyo Ku, Kyoto 6060962, Japan
Kinugawa, Ryoko
Ishihara, Takashi
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Kyoto Inst Technol, Dept Chem & Mat Technol, Sakyo Ku, Kyoto 6060962, JapanKyoto Inst Technol, Dept Chem & Mat Technol, Sakyo Ku, Kyoto 6060962, Japan
Ishihara, Takashi
Yamada, Shigeyuki
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Tokyo Univ Agr & Technol, Grad Sch Engn, Dept Appl Chem, Koganei, Tokyo 1848588, JapanKyoto Inst Technol, Dept Chem & Mat Technol, Sakyo Ku, Kyoto 6060962, Japan
机构:
Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
Lei, AW
Lu, XY
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Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
Lu, XY
Liu, GS
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Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China