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The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic, their interactions with reaction intermediates. Interested yet? Read on for other articles about 5306-85-4. Category: pyrrolines.

Category: pyrrolines, When developing chemical systems it’s of course important to gain a deep understanding of the chemical reaction process. 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, belongs to pyrrolines compound. In a article, author is SIGMAN, MS, introduce new discover of the category.

THE FIRST IRON-MEDIATED CATALYTIC CARBON-NITROGEN BOND FORMATION – [4+1] CYCLOADDITION OF ALLENYL IMINES AND CARBON-MONOXIDE

Catalytic carbon-nitrogen bond formation was achieved by iron carbonyls in the [4 + 1] cycloaddition of allenyl imines with CO. The Fe(CO)(5) photochemically catalyzed reaction of allenyl imines and CO gives preparatively useful yields of 3-alkylidene-4-pyrrolin-2-ones. These reactions take place under mild conditions and only require fluorescent light! Good control of alkylidene bond stereochemistry is achieved when the terminal allene groups are tert-butyl and methyl. Experiments in the dark show that stoichiometric Fe-2(CO)(9) can mediate [4 + 1] assembly by a purely thermal reaction to give good yields of the pyrrolinone products. These new methods for the construction of 3-alkylidene-4-pyrrolin-2-ones are complimentary to existing procedures and allow for a greater variety of alkylidene substituents.

The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic, their interactions with reaction intermediates. Interested yet? Read on for other articles about 5306-85-4. Category: pyrrolines.

Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem