Diastereoselective synthesis of arylglycine derivatives by cationic palladium(II)-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters.
Org Lett. 2007 Aug 02; 9(16):3077-80.OL

Abstract

A cationic palladium-complex-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl iminoacetates to yield the optically active arylglycine derivatives with moderate to good yield and high diastereoselectivity was developed. This reaction provides a convenient and efficient method for the synthesis of arylglycine derivatives.

Authors+Show Affiliations

Dai H

State Key Laboratory of Organometallic Chemistry, Shanghai, Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China.

Lu X

No affiliation info available

MeSH

Boronic AcidsCatalysisEstersGlycineMolecular StructurePalladiumStereoisomerismSulfonium Compounds

Pub Type(s)

Journal Article

Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

17608432

Citation

Dai, Huixiong, and Xiyan Lu. "Diastereoselective Synthesis of Arylglycine Derivatives By Cationic palladium(II)-catalyzed Addition of Arylboronic Acids to N-tert-butanesulfinyl Imino Esters." Organic Letters, vol. 9, no. 16, 2007, pp. 3077-80.

Dai H, Lu X. Diastereoselective synthesis of arylglycine derivatives by cationic palladium(II)-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters. Org Lett. 2007;9(16):3077-80.

Dai, H., & Lu, X. (2007). Diastereoselective synthesis of arylglycine derivatives by cationic palladium(II)-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters. Organic Letters, 9(16), 3077-80.

Dai H, Lu X. Diastereoselective Synthesis of Arylglycine Derivatives By Cationic palladium(II)-catalyzed Addition of Arylboronic Acids to N-tert-butanesulfinyl Imino Esters. Org Lett. 2007 Aug 2;9(16):3077-80. PubMed PMID: 17608432.

* Article titles in AMA citation format should be in sentence-case

TY - JOUR T1 - Diastereoselective synthesis of arylglycine derivatives by cationic palladium(II)-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters. AU - Dai,Huixiong, AU - Lu,Xiyan, Y1 - 2007/07/03/ PY - 2007/7/5/pubmed PY - 2007/9/5/medline PY - 2007/7/5/entrez SP - 3077 EP - 80 JF - Organic letters JO - Org Lett VL - 9 IS - 16 N2 - A cationic palladium-complex-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl iminoacetates to yield the optically active arylglycine derivatives with moderate to good yield and high diastereoselectivity was developed. This reaction provides a convenient and efficient method for the synthesis of arylglycine derivatives. SN - 1523-7060 UR - https://www.unboundmedicine.com/medline/citation/17608432/Diastereoselective_synthesis_of_arylglycine_derivatives_by_cationic_palladium_II__catalyzed_addition_of_arylboronic_acids_to_N_tert_butanesulfinyl_imino_esters_ L2 - https://doi.org/10.1021/ol0711220 DB - PRIME DP - Unbound Medicine ER -

Tags

Diastereoselective synthesis of arylglycine derivatives by cationic palladium(II)-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters.Org Lett. 2007 Aug 02; 9(16):3077-80.OL