A stereoselective synthesis of (+)-boronolide is described. The key steps involve a stereoselective reduction of an oc-hydroxy ketone, allylation of an alpha-hydroxy aldehyde and a ring-closing olefin metathesis of a homoallylic alcohol derived acrylate ester utilizing Grubbs' catalyst. (C) 2000 Elsevier Science Ltd. All rights reserved.
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Univ Jaume 1, UP Quim Inorgan & Organ, E-12080 Castellon de La Plana, SpainUniv Jaume 1, UP Quim Inorgan & Organ, E-12080 Castellon de La Plana, Spain
Carda, M
Rodríguez, S
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机构:Univ Jaume 1, UP Quim Inorgan & Organ, E-12080 Castellon de La Plana, Spain
Rodríguez, S
Segovia, B
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机构:Univ Jaume 1, UP Quim Inorgan & Organ, E-12080 Castellon de La Plana, Spain
Segovia, B
Marco, JA
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机构:Univ Jaume 1, UP Quim Inorgan & Organ, E-12080 Castellon de La Plana, Spain
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Indian Inst Chem Technol, Organ Div 1, Hyderabad 500007, Andhra Pradesh, IndiaIndian Inst Chem Technol, Organ Div 1, Hyderabad 500007, Andhra Pradesh, India
Raghavan, Sadagopan
Krishnaiah, V.
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Indian Inst Chem Technol, Organ Div 1, Hyderabad 500007, Andhra Pradesh, IndiaIndian Inst Chem Technol, Organ Div 1, Hyderabad 500007, Andhra Pradesh, India
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Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R China
Hu, SG
Hu, TS
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Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R China
Hu, TS
Wu, YL
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Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R ChinaChinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R China