<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>DSpace Collection:</title>
  <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/965" />
  <subtitle />
  <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/965</id>
  <updated>2025-10-30T07:10:15Z</updated>
  <dc:date>2025-10-30T07:10:15Z</dc:date>
  <entry>
    <title>Synthesis of D-Fructose-Based Bifunctional Primary Amine-Thiourea Organocatalysts and Their Applications in Asymmetric Reactions</title>
    <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/966" />
    <author>
      <name>Lalhriatpuia, C</name>
    </author>
    <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/966</id>
    <updated>2025-10-16T08:40:44Z</updated>
    <published>2023-10-16T00:00:00Z</published>
    <summary type="text">Title: Synthesis of D-Fructose-Based Bifunctional Primary Amine-Thiourea Organocatalysts and Their Applications in Asymmetric Reactions
Authors: Lalhriatpuia, C
Abstract: The preparation of a new class of six bifunctional thiourea organocatalysts having a Dfructose scaffold and a primary amino group was demonstrated. In the present study, the novel&#xD;
organocatalysts exhibited excellent enantio- and moderate diastereoselectivities in the asymmetric&#xD;
Michael addition of aliphatic ketones and 1,3-diketone to substituted nitroolefins at room temperature.&#xD;
In addition, the direct asymmetric aldol reaction between cyclic aliphatic ketone and aromatic&#xD;
aldehydes was also studied in the presence of the saccharide-thiourea organocatalysts giving excellent&#xD;
yield with moderate enantioselectivity.</summary>
    <dc:date>2023-10-16T00:00:00Z</dc:date>
  </entry>
</feed>

