Stereoselektive Alkylierung an C(α) von Serin, Glycerinsäure, Threonin und Weinsäure über heterocyclische Enolate mit exocyclischer Doppelbindung

Abstract

Steroselective Alkylation at C(α) of Serine, Clyceric Acid, Threonine, and Tartaric Acid Involving Heterocyclic Enolates with Evocyelic Double Bonds The chiral, non‐racemic title acids are converted to methyl dioxolane‐( cf. 13 ), oxazoline‐( 4 ) and oxazolidinecarboxylates ( cf. 9 ). Deprotonation by Li(i‐Pr) 2 N at dry‐ice temperature gives solutions of the lithium enolates A–D With exocyclic enolate double bonds. These are stable crough with respect to β‐elimination ( Scheme 1 ) to be alkylated with or without cosolvents such as HMPA or DMPU The products are formed in good to excellent yields and, with the exception of the tartrate‐derived acetonlde ( see Scheme 2 ), with diastereoselectivities above 90%. While the tartrate‐and threonine‐derived enolates ( A and B , resp.) are chiral due to the second stereogenic center of the precursors, the serine‐ and glyceric‐acid‐derived enolates ( A and B , resp.) are chiral due to the second sterogenic center of the precursors, the serine‐nd glyceric‐acid‐derived enolates are non‐racemic due to a tert butyl‐substituted (pivalaldehyde‐derived) acetal center ( C and D , resp.). The products of alkylation can be hydrolyzed to give α‐branched tartaric acid ( Scheme 2 ), allothreonine ( Scheme 3 ), serine ( Scheme 4 ), and glyceric‐acid derivatives ( Scheme 5 ) with quaternary stereogenic centers. The configurations of the products are determined by NOE‐NMR measurements and by chemical correlation. These show that the dioxolane‐derived enolates A and D are alkylated preferentially from that face of the ring which is already substituted (‘ syn ’‐attack), while the dihydrooxazol‐and oxazolidine‐derived enolates B and C are alkylated from the opposite face (‘ anti ’‐attack). The ‘ syn ’‐attack is postulated to arise from strong folding of the heterocyclic ring due to electronic repulsion between the enolate π‐system and non‐bonding electron pairs on the heteroatoms ( see Scheme 6 ).

Keywords

Affiliated Institutions

• Sanden (Japan) JP
• Roche (Switzerland) CH

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