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Macromolecules, ISSN 0024-9297, 09/2008, Volume 41, Issue 17, pp. 6361 - 6366
Highly refractive and transparent polyimides (PIs) containing a 3,4,8,9-tetrahydro-2,5,7,10-tetrathiaanthracene moiety in their main chains have been... 
TETRACARBOXYLIC DIANHYDRIDES | POLYMER SCIENCE | DIAMINES | LIGHT
Journal Article
Tetrahedron, ISSN 0040-4020, 07/2013, Volume 69, Issue 26, pp. 5299 - 5305
Reaction of Woollins' reagent (WR) with trans-1,2-cyclohexanediamine or 1,3-cyclohexanediamine, followed by treatment with o-xylylenedibromide in THF at room... 
Diamines | X-rays | Tetrahedrons
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 11/2019, Volume 60, Issue 46, p. 151247
The Mannich reaction of pyrrole with ethylenediamine dihydrochloride and formaldehyde gave two compounds: -tetrakis(pyrrol-2-ylmethyl)ethane-1,2-diamine and... 
Diamine | Mannich reaction | Pyrrole | Macrocycle
Journal Article
Journal of Applied Polymer Science, ISSN 0021-8995, 04/2013, Volume 128, Issue 1, pp. 566 - 571
Polyurethanes were prepared via a nonisocyanate route, by reacting carbonated soybean oil (CSBO) with aromatic and cycloaliphatic diamines. Nonisocyanate... 
soy oil | diamine | polyurethane | aromatic | non‐isocyanate | non-isocyanate | POLYADDITION | POLYMER SCIENCE | CYCLIC CARBONATE | CARBON-DIOXIDE | Mechanical properties | Toluene diamine | Urethanes | Carbonates | Toluene | Polyurethane resins | Diamines | Amines | Swelling | Computer networks | Aliphatic compounds | Tensile strength
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 12/2012, Volume 58, pp. 581 - 590
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2009, Volume 48, Issue 15, pp. 2777 - 2779
A grand opening: N‐Boc‐N‐alkylsulfamides are effective substrates for the title transformation. Oxidative cyclization is highly chemoselective as well as being... 
amination | CH insertion | sulfamides | diamines | rhodium | Diamines | Sulfamides | Amination | Rhodium | C-H insertion | 1,2,5-THIADIAZOLIDINE | EFFICIENT SYNTHESIS | BOND FORMATION | SULFONAMIDES | 1,1-DIOXIDES | CHEMISTRY, MULTIDISCIPLINARY | FUNCTIONALIZATION | AZIRIDINATION | DIAMINATION | AMINATION REACTIONS | DERIVATIVES | Synthetic Methods | C—H insertion
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2019, Volume 58, Issue 47, pp. 16831 - 16834
A highly enantioselective iridium‐ or ruthenium‐catalyzed intermolecular reductive amination/asymmetric hydrogenation relay with 2‐quinoline aldehydes and... 
vicinal diamines | reductive amination | asymmetric hydrogenation | tandem reactions | N-heterocyclic carbenes | Diamines | Ruthenium | Amines | Asymmetry | Amination | Metathesis | Quinoline | Iridium | Aldehydes | Enantiomers | Hydrogenation | Carbenes
Journal Article
RSC Advances, 01/2019, Volume 9, Issue 29, pp. 16384 - 16389
Here, we have described the synthesis of novel spiropyridineoxindole derivatives containing a pyridone ring via a four-component reaction between various... 
Diamines | Synthesis | Ethanol | Derivatives
Journal Article
Organic Letters, ISSN 1523-7060, 01/2016, Volume 18, Issue 2, pp. 300 - 303
A well-defined nonprecious metal cobalt­(II) catalyst based on a pincer PNP ligand has been employed for the efficient N-alkylation of both aromatic and... 
KETONES | MILD REACTION CONDITIONS | DEHYDROGENATION | DIAMINES | CHEMISTRY, ORGANIC | TRANSFER HYDROGENATION | ACCEPTOR-LESS | C=N BONDS | EFFICIENT | IRIDIUM CATALYSTS | AROMATIC-AMINES
Journal Article
Journal Article
11/2010
The chiral vicinal diamine moiety is “privileged” and is widely found in catalysts and bio-active compounds. A series of seven chiral vicinal diamines with... 
chemistry | optical purity | synthesis | amino acid | diamine | vicinal diamine | stereoselective | heterocycle | 0490 | guanidine | chiral shift reagent | NMR | 0487 | enantiomer | chiral diamine | organic
Dissertation
International Journal of Radiation Oncology, Biology, Physics, ISSN 0360-3016, 2012, Volume 82, Issue 5, pp. e701 - e707
Purpose A new aminothiol, PrC-210, was tested for orally conferred radioprotection (rats, mice; 9.0 Gy whole-body, which was otherwise lethal to 100% of the... 
Radiology | Hematology, Oncology and Palliative Medicine | Oral radioprotection | Amifostine toxicity | Survival assay | Aminothiol | PrC-210 | TRIAL | ONCOLOGY | AGENTS | WR-2721 | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | CHEMOTHERAPY | RADIATION-THERAPY | Sulfhydryl Compounds - administration & dosage | Nausea - chemically induced | Radiation-Protective Agents - pharmacokinetics | Radiation-Protective Agents - administration & dosage | Male | Radiation Injuries, Experimental - prevention & control | Diamines - adverse effects | Diamines - pharmacokinetics | Injections, Subcutaneous | Diamines - administration & dosage | Female | Sulfhydryl Compounds - chemistry | Drug Evaluation, Preclinical | Administration, Oral | Infusions, Parenteral | Radiation-Protective Agents - chemistry | Rats | Ferrets | Hypotension - chemically induced | Rats, Sprague-Dawley | Sulfhydryl Compounds - pharmacokinetics | Mice, Inbred ICR | Vomiting - chemically induced | Maximum Tolerated Dose | Sulfhydryl Compounds - adverse effects | Animals | Amifostine - administration & dosage | Diamines - chemistry | Mice | Radiation-Protective Agents - adverse effects | Infusions, Intra-Arterial | Complications and side effects | Fainting | Oncology, Experimental | Nausea | Research | Hypotension | Cancer | HUMAN POPULATIONS | IRRADIATION | VOMITING | DRUGS | HYPOTENSION | NAUSEA | RATS | RADIOLOGY AND NUCLEAR MEDICINE | MICE | RADIATION DOSES | TOXICITY | SIDE EFFECTS
Journal Article