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Synthesis of non-racemic α-hydroxyphosphonates via asymmetric phospho-aldol reaction.
Top Curr Chem. 2015; 361:83-136.TC

Abstract

It has been more than 50 years since the first phospho-aldol reactions of dialkyl phosphites were reported. These efficient P-C bond-forming reactions have become the cornerstone of methods for the synthesis of α-hydroxyphosphonates and, by numerous available substitution reactions, the synthesis of other α- and γ-substituted phosphonates and phosphonic acids. Much of the interest in α- and γ-substituted phosphonates and phosphonic acids has been stimulated by reports of their biological activity, which is often dependent upon their absolute and relative stereochemistry. In this chapter, we review diastereoselective and enantioselective additions of dialkyl phosphites to aldehydes and ketones, otherwise called the phospho-aldol, Pudovik or Abramov reactions.

Authors+Show Affiliations

Department of Chemistry and Biochemistry, University of Missouri-St. Louis, One University Boulevard, St. Louis, MO, 63121, USA, cspill@umsl.edu.No affiliation info available

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

25467537

Citation

Spilling, Christopher D., and Raj K. Malla. "Synthesis of Non-racemic Α-hydroxyphosphonates Via Asymmetric Phospho-aldol Reaction." Topics in Current Chemistry, vol. 361, 2015, pp. 83-136.
Spilling CD, Malla RK. Synthesis of non-racemic α-hydroxyphosphonates via asymmetric phospho-aldol reaction. Top Curr Chem. 2015;361:83-136.
Spilling, C. D., & Malla, R. K. (2015). Synthesis of non-racemic α-hydroxyphosphonates via asymmetric phospho-aldol reaction. Topics in Current Chemistry, 361, 83-136. https://doi.org/10.1007/128_2014_583
Spilling CD, Malla RK. Synthesis of Non-racemic Α-hydroxyphosphonates Via Asymmetric Phospho-aldol Reaction. Top Curr Chem. 2015;361:83-136. PubMed PMID: 25467537.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Synthesis of non-racemic α-hydroxyphosphonates via asymmetric phospho-aldol reaction. AU - Spilling,Christopher D, AU - Malla,Raj K, PY - 2014/12/4/entrez PY - 2014/12/4/pubmed PY - 2015/6/3/medline SP - 83 EP - 136 JF - Topics in current chemistry JO - Top Curr Chem VL - 361 N2 - It has been more than 50 years since the first phospho-aldol reactions of dialkyl phosphites were reported. These efficient P-C bond-forming reactions have become the cornerstone of methods for the synthesis of α-hydroxyphosphonates and, by numerous available substitution reactions, the synthesis of other α- and γ-substituted phosphonates and phosphonic acids. Much of the interest in α- and γ-substituted phosphonates and phosphonic acids has been stimulated by reports of their biological activity, which is often dependent upon their absolute and relative stereochemistry. In this chapter, we review diastereoselective and enantioselective additions of dialkyl phosphites to aldehydes and ketones, otherwise called the phospho-aldol, Pudovik or Abramov reactions. SN - 0340-1022 UR - https://www.unboundmedicine.com/medline/citation/25467537/Synthesis_of_non_racemic_α_hydroxyphosphonates_via_asymmetric_phospho_aldol_reaction_ DB - PRIME DP - Unbound Medicine ER -