(Q60458522)

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Aldol reactions in polypropionate synthesis: High π-face selectivity of enol borinates from α-chiral methyl and ethyl ketones under substrate control

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scholarly article

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Aldol reactions in polypropionate synthesis: High π-face selectivity of enol borinates from α-chiral methyl and ethyl ketones under substrate control (English)

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Jonathan M. Goodman

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Jonathan M. Goodman

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author name string

Ian Paterson

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Masahiko Isaka

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publication date

1989

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Tetrahedron Letters

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30

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50

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7121-7124

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Major effect of the leaving group in dialkylboron chlorides and triflates in controlling the stereospecific conversion of ketones into either [E]- or [Z]-enol borinates

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https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2993440-9

7 January 2021

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Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates

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https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2993440-9

7 January 2021

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Stereoselective aldol condensations via boron enolates

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https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2993440-9

7 January 2021

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Aldol reactions of methylketones using chiral boron reagents: A reversal in aldehyde enantioface selectivity

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https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2993440-9

7 January 2021

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Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydride

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https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2993440-9

7 January 2021

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Identifiers

10.1016/S0040-4039(01)93440-9

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