苄氧基丙酮
苄氧基丙酮结构式
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常用名 | 苄氧基丙酮 | 英文名 | 1-(Benzyloxy)acetone |
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| CAS号 | 22539-93-1 | 分子量 | 164.201 | |
| 密度 | 1.0±0.1 g/cm3 | 沸点 | 268.4±15.0 °C at 760 mmHg | |
| 分子式 | C10H12O2 | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | 116.0±13.9 °C |
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Cis selective wittig olefination of a-alkoxy ketones and its application to the stereoselective synthesis of plaunotol. Inoue S, et al.
Bull. Chem. Soc. Jpn. 63(6) , 1629-1635, (1990)
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Highly selective direct aldol reaction organocatalyzed by (S)-BINAM-L-prolinamide and benzoic acid using a-chalcogen-substituted ketones as donors. Guillena G, et al.
ARKIVOC 4 , 260-269, (2007)
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A stereoselective formation of (Z)-2-methyl-2-alkenol by the wittig reaction: its application to a synthesis of nerylacetone and (Z,Z)-farnesylacetone. Sato K, et al.
Chem. Lett. 10(12) , 1711-1714, (1981)
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Stereochemical control of bakers' yeast mediated reduction of a protected 2-hydroxy ketone. Manzocchi A, et al.
J. Org. Chem. 53(18) , 4405-4407, (1988)
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Synthesis and biological evaluation of Bioorg. Med. Chem. Lett. 11(17) , 2301-2304, (2001)
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