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Volumn 28, Issue 25, 1987, Pages 2841-2844

Double asymmetric aldol reactions using the boron enolates derived from 3-(3-ethyl)pentyl propanethiote and ethanethioate with (R,R)-2,5-dimethylborolanyl triflate

(2) Short, Robert P a Masamune, Satoru a

a MASSACHUSETTS INSTITUTE OF TECHNOLOGY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0013372519 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)96223-3 Document Type: Article

Times cited : (34)

References (20)

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4
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8
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9
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- Enantio- andanti-Diastereoselective Aldol Additions of Acetates and Propionates viaO-Silyl Ketene Acetals
- Int. Ed. Engl.
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13
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- Highly enantioselective synthesis of anti(threo)-aldols by the asymmetric aldol reaction utilizing a chiral azaenolate.
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- Narasaka¹ Miwa²

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- Directed Homogeneous Hydrogenation[New Synthetic Methods(65)]
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16
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17
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18
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- 13C chemical shift for C-3 is assigned the 3,4-anti structure. These values reflect an apparent equatorial orientation for the thioester side chain in the 3,4-anti products and an axial orientation for this substituent in the 3,4-syn product. See the Table for complete spectral data on these compounds.

19
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