JOURNAL ARTICLE

Synthesis of Enantiomerically Pure 1,2-Disubstituted 2-Selenoamines

Esther TorrenteGarcia LuisA. M. Martín-CastroAlessandro Degl’InnocentiAntonella CapperucciLucrezia Frateschi

Year: 2011 Journal:   Phosphorus, sulfur, and silicon and the related elements Vol: 186 (5)Pages: 1268-1273   Publisher: Taylor & Francis

Abstract

Optically pure phenylseleno-(S)-2-p-tolylsulfinylbenzylcarbanions react with (S)-N-2-p-tolylsulfinylimines derived from aliphatic and aromatic aldehydes in a highly stereoselective manner affording bis-sulfinylselenoamines, easily transformed into 1-phenyl, 2-aryl (or alkyl)-2-phenylseleno ethylamines by subsequent reactions, which were treatment reactions with t-BuLi and TFA

Keywords:
Chemistry Alkyl Sulfur Stereoselectivity Aryl Phosphorus Organic chemistry Medicinal chemistry Silicon Catalysis

Metrics

2
Cited By
0.19
FWCI (Field Weighted Citation Impact)
27
Refs
0.49
Citation Normalized Percentile
Is in top 1%
Is in top 10%

Citation History

Topics

Organoselenium and organotellurium chemistry
Life Sciences →  Pharmacology, Toxicology and Pharmaceutics →  Toxicology
Sulfur-Based Synthesis Techniques
Physical Sciences →  Chemistry →  Organic Chemistry
Organophosphorus compounds synthesis
Physical Sciences →  Chemistry →  Organic Chemistry

Related Documents

© 2026 ScienceGate Book Chapters — All rights reserved.