Highly diastereoselective reduction and alkylation of (1R,2S)-trans-2-phenylcyclohexanol phenylglyoxylate and pyruvate using hindered hydrides and alkyl aluminates
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作者:
Boireau, G
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Univ Paris 11, Inst Chim Mol Orsay, Lab React Select Supports, F-91405 Orsay, FranceUniv Paris 11, Inst Chim Mol Orsay, Lab React Select Supports, F-91405 Orsay, France
Boireau, G
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Deberly, A
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Univ Paris 11, Inst Chim Mol Orsay, Lab React Select Supports, F-91405 Orsay, FranceUniv Paris 11, Inst Chim Mol Orsay, Lab React Select Supports, F-91405 Orsay, France
Deberly, A
[1
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Loupy, A
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Univ Paris 11, Inst Chim Mol Orsay, Lab React Select Supports, F-91405 Orsay, FranceUniv Paris 11, Inst Chim Mol Orsay, Lab React Select Supports, F-91405 Orsay, France
Loupy, A
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Monteux, D
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Univ Paris 11, Inst Chim Mol Orsay, Lab React Select Supports, F-91405 Orsay, FranceUniv Paris 11, Inst Chim Mol Orsay, Lab React Select Supports, F-91405 Orsay, France
Monteux, D
[1
]
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[1] Univ Paris 11, Inst Chim Mol Orsay, Lab React Select Supports, F-91405 Orsay, France
(1R,2S)-trans-2-Phenylcyciohexanol phenylglyoxylate and pyruvate are reduced with modest to excellent diastereoselectivities (30-99%) by reaction with bulky lithium trialkoxyaluminohydrides and alkylated with excellent diastereoselectivities (88-100%) by addition of hindered lithium alkoxytrialkylaluminates. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.