Chemical Research Letters, May 2021. The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 5306-85-4, Name is (3R,3aR,6S,6aR)-3,6-Dimethoxyhexahydrofuro[3,2-b]furan, SMILES is CO[C@H]1CO[C@@]2([H])[C@]1([H])OC[C@H]2OC, in an article , author is Mahboobi, S, once mentioned of 5306-85-4, Name: (3R,3aR,6S,6aR)-3,6-Dimethoxyhexahydrofuro[3,2-b]furan.
Synthesis of pyrrolo[3 ‘,3 ‘: 2,3]azepino[4,5,6-cd]indol-8,10-diones
3-Amino-4-(3-indolyl)pyrrolin-2,5-diones are condensed with various aldehydes and ketones to the corresponding imines. Under Pietet-Spengler conditions, the latter do not cyclize to pyrrolo-beta -carbolines, but readily yield pyrrolo[3′,4’:2,3]azepino[4,5,6-cd]indole-8,10-diones.
The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’ molecules. In my other articles, you can also check out more blogs about 5306-85-4. Name: (3R,3aR,6S,6aR)-3,6-Dimethoxyhexahydrofuro[3,2-b]furan.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem