Synthesis of chiral Nβ-protected amino diselenides from the corresponding amino alkyl iodides using NaBH2Se3 as a selenating reagent and their conversion to seleninic acids-Reference-Cited by-同舟云学术

Synthesis of chiral Nβ-protected amino diselenides from the corresponding amino alkyl iodides using NaBH2Se3 as a selenating reagent and their conversion to seleninic acids

Published:2015 Issue:64 Volume:5 Page:51807-51811
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Panguluri Nageswara Rao¹²³⁴⁵,Panduranga Veladi¹²³⁴⁵,Prabhu Girish¹²³⁴⁵,Vishwanatha T. M.¹²³⁴⁵,Sureshbabu Vommina V.¹²³⁴⁵

Affiliation:

1. Peptide Research Laboratory

2. Department of Studies in Chemistry

3. Bangalore University

4. Bangalore 560 001

5. India

Abstract

Synthesis of N^β-protected amino diselenides and l-selenocystine methyl esters from amino alkyl iodides using NaBH₂Se₃ as an efficient selenating reagent is described. Further the synthesis of N^β-protected amino seleninic acids using 35% aqueous H₂O₂ has been demonstrated.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA06147D

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