On January 16, 2015, Amaral, Monica F. Z. J.; Baumgartner, Amanda A.; Vessecchi, Ricardo; Clososki, Giuliano C. published an article.Product Details of 93476-46-1 The title of the article was Directed Metalation of 1-Ester-Substituted Indolizines: Base/Electrophile-Controlled Regioselective Functionalization. And the article contained the following:
A variety of C-2 and C-5 difunctionalized indolizines e. g., I, have been prepared through the reaction of 1-ester-substituted indolizines with organometallic bases followed by a reaction with different electrophiles. Metalation takes place under mild conditions allowing the isolation of a number of difunctionalized indolizines in good yields. The regioselectivity of the reaction appears to be governed by the nature of the base and electrophile. The experimental process involved the reaction of Ethyl indolizine-1-carboxylate(cas: 93476-46-1).Product Details of 93476-46-1
The Article related to indolizine regioselective synthesis, electrophile indolizine organometallic base metalation, Heterocyclic Compounds (One Hetero Atom): Pyridines and other aspects.Product Details of 93476-46-1
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics