A new chemoenzymatic Baylis-Hillman approach for the synthesis of enantiomerically enriched umbelactones
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作者:
Kamal, Ahmed
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Indian Inst Chem Technol, Div Organ Chem, Biotransformat Lab, Hyderabad 500007, Andhra Pradesh, IndiaIndian Inst Chem Technol, Div Organ Chem, Biotransformat Lab, Hyderabad 500007, Andhra Pradesh, India
Kamal, Ahmed
[1
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Krishnaji, Tadiparthi
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Indian Inst Chem Technol, Div Organ Chem, Biotransformat Lab, Hyderabad 500007, Andhra Pradesh, IndiaIndian Inst Chem Technol, Div Organ Chem, Biotransformat Lab, Hyderabad 500007, Andhra Pradesh, India
Krishnaji, Tadiparthi
[1
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Reddy, P. Venkat
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Indian Inst Chem Technol, Div Organ Chem, Biotransformat Lab, Hyderabad 500007, Andhra Pradesh, IndiaIndian Inst Chem Technol, Div Organ Chem, Biotransformat Lab, Hyderabad 500007, Andhra Pradesh, India
Reddy, P. Venkat
[1
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[1] Indian Inst Chem Technol, Div Organ Chem, Biotransformat Lab, Hyderabad 500007, Andhra Pradesh, India
An efficient and convenient strategy for the enantioselective synthesis of enantiomerically enriched umbelactones is described utilizing a lipase-mediated resolution protocol, Baylis-Hillman reaction and ring closing metathesis as key steps. The lipase-resolution is carried out using several lipases from various sources in different solvents to afford the required intermediate 8 in good yield and high enantioselectivity. (C) 2007 Elsevier Ltd. All rights reserved.
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Abbott Labs, Global Pharmaceut Res & Dev, Enabling Chem Technol, Abbott Pk, IL 60064 USAAbbott Labs, Global Pharmaceut Res & Dev, Enabling Chem Technol, Abbott Pk, IL 60064 USA
Vasudevan, Anil
Tseng, Pei-San
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Abbott Labs, Global Pharmaceut Res & Dev, Enabling Chem Technol, Abbott Pk, IL 60064 USAAbbott Labs, Global Pharmaceut Res & Dev, Enabling Chem Technol, Abbott Pk, IL 60064 USA
Tseng, Pei-San
Djuric, Stevan W.
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Abbott Labs, Global Pharmaceut Res & Dev, Enabling Chem Technol, Abbott Pk, IL 60064 USAAbbott Labs, Global Pharmaceut Res & Dev, Enabling Chem Technol, Abbott Pk, IL 60064 USA