698353-37-6

Upstream product

• 698353-48-9 C₂₁H₂₆N₂ 
• 121-46-0 bicyclo[2.2.1]hepta-2,5-diene 
• 16473-11-3 bicyclo[3.3.1]nonane-2,6-dione 
• 171065-84-2 2,5-diaminobicyclo[2.2.1]heptane 
• 141737-16-8 rac-bicyclo[2.2.1]heptane-2,5-dione dioxime 
• 145092-68-8 (S,S)-bicyclo<2.2.1>heptane-2,5-dione 
• 121-46-0 bicyclo[2.2.1]hepta-2,5-diene 
• 5888-36-8 (1S,2R,4S,5R)-2,5-dihydroxybicyclo[2.2.1]heptane 
• 698353-40-1 (1S,2S,4S,5S)-2,5-bis[(4-methylphenyl)sulfonylamido]bicyclo[2.2.1]heptane 
• 145092-77-9 (1R,4R)-bicyclo[2.2.1]heptane-2,5-dione 
• 135094-36-9 (1R,2S,4R,5S)-exo,exo-bicyclo[2.2.1]heptane-2,5-diol 
• 698353-39-8 (1R,2R,4R,5R)-2,5-bis[(4-methylphenyl)sulfonylamido]bicyclo[2.2.1]heptane 
• 1379292-26-8 bicyclo[2.2.1]heptane-2,6-dicarboamide 
• 1379301-92-4 bicyclo[2.2.1]heptane-2,5-dicarboamide 

Downstream Products

• 698353-43-4 (1R,2R,4R,5R)-2,5-diaminobicyclo[2.2.1]heptane 
• 698353-42-3 (1S,2S,4S,5S)-2,5-diamino-bicyclo[2.2.1]heptane 

Relevant academic research and scientific papers

MODULATORS OF THE INTEGRATED STRESS PATHWAY

Provided herein are compounds, compositions, and methods useful for the modulation of elF2B, for modulating the integrated stress response (ISR) and for treating related diseases; disorders and conditions.

Evaluation of the chiral DIANANE backbone as ligand for organolithium reagents

Novel endo,endo-2,5-diaminonorbonane-derived tertiary C2- symmetrical diamines were synthesized via the one-pot reductive amination of enantiomerically pure norbornane-2,5-dione. These ligands were applied to various catalytic reactions such as asymmetric deprotonation, asymmetric bromine-lithium exchange, and enantioselective addition of aryl- and allkylithium reagents to aromatic aldimines. Copyright

Novel polyisocyanate compound, method for producing the same, and uses thereof

The invention provides an optical material being excellent in balance between the heat resistance, Abbe number and refractive index by providing a compound represented by the general formula (1): in the formula, k and n representing integers of 0 to 2 and 0 to 1, respectively, with the proviso that k and n are not simultaneously zero, and k=0 meaning that —(CH2)k- is not included in the formula.

Enantioselective Synthesis of DIANANE, a Novel C2-Symmetric Chiral Diamine for Asymmetric Catalysis

DIANANE (endo,endo-2,5-diaminonorbornane) is a novel chiral C 2-symmetric diamine, based on the rigid bicyclo[2.2.1]heptane scaffold. Schiff-base ligands derived from DIANANE have already found use in asymmetric catalysis, e.g., in the highly e

A highly enantioselective catalyst for the asymmetric Nozaki-Hiyama-Kishi reaction of allylic and vinylic halides

Catalytic asymmetric addition of vinylic halides and trifiates to aldehydes, with useful levels of stereoinduction, has been achieved for the first time using the salentype ligand (S,S)-5 (see scheme; PMB=para-methoxybenzyl), which contains the novel endo