Regioselective 2-Imino-1,3-thiazolidine vs. 2-Imino-1,3-oxazolidine Formation from the Vicinalsec-Amino Alcohol of Desosamine
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201300266/fullpdf
Reference17 articles.
1. Novel Tandem Reaction for the Synthesis of N′-Substituted 2-Imino-1,3-oxazolidines from Vicinal (sec- or tert-)Amino Alcohol of Desosamine
2. Novel desosamine-modified 14- and 15-membered macrolides without antibacterial activity
3. N′-Substituted-2′-O,3′-N-carbonimidoyl Bridged Macrolides: Novel Anti-inflammatory Macrolides without Antimicrobial Activity
4. Facile and Efficient Guanylation of Amines Using Thioureas and Mukaiyama's Reagent
5. Synthetic approaches towards 2-iminothiazolidines: an overview
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1. CS2/CO2 Utilization Using Mukaiyama Reagent as a (Thio)carbonylating Promoter: A Proof-of-Concept Study;ACS Omega;2022-06-21
2. Synthetic Routes to 2-Iminothiazolidines: State-of-the-Art 2006-2020;Current Organic Chemistry;2020-12-31
3. On Water: Metal-Free Synthesis of Highly Functionalized Benzothiazolylidene from ortho-Haloanilines;The Journal of Organic Chemistry;2019-01-31
4. Asymmetric Synthesis of 2-Thiocyanato-2-(1-aminoalkyl)-substituted 1-Tetralones and 1-Indanones with Tetrasubstituted Carbon Stereogenic Centers via Cooperative Cation-Binding Catalysis;Advanced Synthesis & Catalysis;2017-04-28
5. One-Pot Three-Component Synthesis of 2-Imino-1,3-Thiazolines on Soluble Ionic Liquid Support;ACS Combinatorial Science;2016-09-21
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