| Total synthesis of 5R,5-(1''''R-hydroxy-2''''-phenylethyl)-γ-lactone |
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| 引用本文： | YU,Li-Bing WANG,Zhi-QinShanghai Institute of Organic Chemistry,Chinese Academy of Sciences,354 Fenglin Lu,Shanghai 200032,China. Total synthesis of 5R,5-(1''''R-hydroxy-2''''-phenylethyl)-γ-lactone[J]. 中国化学, 1994, 12(6): 524-527. DOI: 10.1002/cjoc.19940120607 |
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| 作者姓名： | YU Li-Bing WANG Zhi-QinShanghai Institute of Organic Chemistry Chinese Academy of Sciences 354 Fenglin Lu Shanghai 200032 China |
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| 作者单位： | YU，Li-Bing WANG，Zhi-QinShanghai Institute of Organic Chemistry，Chinese Academy of Sciences，354 Fenglin Lu，Shanghai 200032，China |
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| 摘 要： | The latest and highly efficient asymmetric dihydroxylation was employed to create the chiral vicinal dihydroxy group of the title compound 1, which has been synthesized from phenylacetaldehyde through 6 steps with a total yield of 61%.
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Total synthesis of 5R,5-(1′R-hydroxy-2′-phenylethyl)-γ-lactone |
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| YU,Li-Bing WANG,Zhi-Qin. Total synthesis of 5R,5-(1′R-hydroxy-2′-phenylethyl)-γ-lactone[J]. Chinese Journal of Chemistry, 1994, 12(6): 524-527. DOI: 10.1002/cjoc.19940120607 |
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| Authors: | YU Li-Bing WANG Zhi-Qin |
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| Affiliation: | YU,Li-Bing WANG,Zhi-QinShanghai Institute of Organic Chemistry,Chinese Academy of Sciences,354 Fenglin Lu,Shanghai 200032,China |
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| Abstract: | The latest and highly efficient asymmetric dihydroxylation was employed to create the chiral vicinal dihydroxy group of the title compound 1, which has been synthesized from phenylacetaldehyde through 6 steps with a total yield of 61%. |
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| Keywords: | Total synthesis asymmetric dihydroxylation 5R 5-(1' R-hydroxy-2'-phenylethyl)-r-lactone. |
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