Stereoselective synthesis of benzosulfamidate-fused tetrahydroquinazoline scaffold via organocatalytic [4+2] cycloaddition of 2-amino-β-nitrostyrenses of cyclic N-sulfimines-Reference-Cited by-同舟云学术

Stereoselective synthesis of benzosulfamidate-fused tetrahydroquinazoline scaffold via organocatalytic [4+2] cycloaddition of 2-amino-β-nitrostyrenses of cyclic N-sulfimines

Published:2016-12 Issue:52 Volume:57 Page:5907-5910
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sim Jong-Tack,Kim Hanna,Kim Sung-Gon

Funder

National Research Foundation of Korea

Ministry of Education

Nanomaterial Technology Development Program

Ministry of Science, ICT and Future Planning

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

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5. Asymmetric Synthesis of 2,3-Dihydro-2-arylquinazolin-4-ones: Methodology and Application to a Potent Fluorescent Tubulin Inhibitor with Anticancer Activity

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