Iodine-Mediated Cyclization of (4R,5R)-4,5-Diamino-N,N′-bis[(1S)-1-phenylethyl]-1,7-octadiene - A Stereoselective Route to 2,5-Diazabicyclo[2.2.1]heptanes
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference69 articles.
1. Synthesis and X-ray Crystal Structure of N,N-Bis[(S)-1-phenylethyl]-(R,R)-4,5- diamino-1,7-octadiene
2. Synthesis ofN,N′-Disubstituted (1R,2R)-1,2-Diaminocyclohex-4-enes by a Ruthenium-Catalyzed Ring-Closing Metathesis Reaction
3. Progress towards the Stereoselective Synthesis of 3,6-Disubstituted 1,2-Diamino-4-cyclohexenes by Ring Closing Metathesis Reaction
4. RCM Approaches toward the Diastereoselective Synthesis of Vicinal trans-Diaminocyclitols from l-Serine
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1. Crystal structure of (1S,4S)-2,5-diazoniabicyclo[2.2.1]heptane dibromide;Acta Crystallographica Section E Crystallographic Communications;2017-11-17
2. Formation of Benzimidazoisoquinolinium and Benzimidazoisoindolinum Cyclic Systems by the Reaction of 2-(2-Alkynylphenyl)benzimidazoles with Iodine and Iodine–Iodine Interaction Including Halogen Bonding in Their Crystal Structures;The Journal of Organic Chemistry;2016-06-15
3. Octa-1,7-diene-4,5-diamine Derivatives: Useful Intermediates for the Stereoselective Synthesis of Nitrogen Heterocycles and Ligands for Asymmetric Catalysis;European Journal of Organic Chemistry;2016-06-14
4. The synthesis and biological evaluation of 1-C-alkyl-l-arabinoiminofuranoses, a novel class of α-glucosidase inhibitors;Bioorganic & Medicinal Chemistry Letters;2011-01
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