Molecules | Free Full-Text | Synergy Effects in the Chemical Synthesis and Extensions of Multicomponent Reactions (MCRs)—The Low Energy Way to Ultra-Short Syntheses of Tailor-Made Molecules | HTML
Triphosgene–pyridine mediated stereoselective chlorination of acyclic aliphatic 1,3-diols - Chemical Communications (RSC Publishing) DOI:10.1039/C5CC06365E
A decade review of triphosgene and its applications in organic reactions - ScienceDirect
Study on Synthesis of Nitrophenyl Isocyanates Using Triphosgene | Scientific.Net
Beyond Chlorine Reagents: Organic Carbonate Chemistry | SpringerLink
Triphosgene and DMAP as Mild Reagents for Chemoselective Dehydration of Tertiary Alcohols
Synthesis of Vinyl Chlorides via Triphosgene–Pyridine Activation of Ketones,The Journal of Organic Chemistry - X-MOL
Solved: 6. Phosgene, Cl2CO, Is A Colorless Gas That Was Us... | Chegg.com
New aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activity
Solved: Could You Please Show This Mechanism With The Incl... | Chegg.com
Bis(trichloromethyl)carbonate (BTC, Triphosgene): A Safer Alternative to Phosgene?
Molecules | Free Full-Text | Cyclization of Hydrazones of 2-Acetyl-1-naphthol and 1-Acetyl-2-naphthol with Triphosgene. Synthesis of Spiro Naphthoxazine Dimers | HTML
Vita — Heiner Eckert
Triphosgene–pyridine mediated stereoselective chlorination of acyclic aliphatic 1,3-diols - Chemical Communications (RSC Publishing) DOI:10.1039/C5CC06365E
New aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activity
α-Amino acid N-Carboxy Anhydrides in pharmaceutical innovations:
Phosgenation reactions
Vita — Heiner Eckert
A REVIEW AND METHODS TO HANDLE PHOSGENE, TRIPHOSGENE SAFELY DURING DRUG SYNTHESIS | New Drug Approvals
In Situ Monitoring of Chemical Reactions – A Molecular Video - - ReactIR
Scheme 9 | Progress in silica polypeptide composite colloidal hybrids: from silica cores to fuzzy shells | SpringerLink
One-pot and novel route for the synthesis of 4-substituted-1,2,4-triazolidine-3,5-diones
