Amine–boranes bearing borane-incompatible functionalities: application to selective amine protection and surface functionalization. Issue 80 (2nd September 2016)

• Record Type: Journal Article
• Authors: Veeraraghavan Ramachandran, P.; Kulkarni, Ameya S.; Zhao, Yan; Mei, Jianguo
• Is Part Of: Chemical communications. Volume 52:Issue 80(2016)
• Page Start: 11885
• Page End: 11888
• Publication Date: 2016-09-02
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1039/c6cc06031e
• Languages: English
• ISSNs: 1359-7345

Abstract

Abstract : The first general open-flask synthesis of amine–boranes with inexpensive and readily available reagents, such as sodium borohydride, sodium bicarbonate, water, and the desired amines is described. Abstract : The first general open-flask synthesis of amine–boranes with inexpensive and readily available reagents, such as sodium borohydride, sodium bicarbonate, water, and the desired amines is described. Even amines bearing borane-reactive functionalities, such as alkene, alkyne, hydroxyl, thiol, ester, amide, nitrile, and nitro are well tolerated. Some of these novel amine–boranes represent stable molecules containing potentially incompatible electrophilic and nucleophilic centers in proximity. This convenient scalable synthesis provides a novel class of organic ligands for surface functionalization, as demonstrated by the formation of self-assembled layers of thiol- and alkoxysilane-bearing amine–boranes on gold and silica surfaces, respectively.