Unsubstituted Bambusurils: Post-Macrocyclization Modification of Versatile Intermediates | Zendy

Václav Havel | Zendy; Tereza Sadilová | Zendy; Vladimír Šindelář | Zendy

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Unsubstituted Bambusurils: Post-Macrocyclization Modification of Versatile Intermediates

Author(s) -

Václav Havel,

Tereza Sadilová,

Vladimír Šindelář

Publication year - 2018

Publication title -

acs omega

Language(s) - Uncategorized

Resource type - Journals

SCImago Journal Rank - 0.779

H-Index - 40

ISSN - 2470-1343

DOI - 10.1021/acsomega.8b00497

Subject(s) - chemistry , derivative (finance) , combinatorial chemistry , copper , surface modification , nitrogen , click chemistry , stereochemistry , medicinal chemistry , polymer chemistry , organic chemistry , financial economics , economics

A new bambusuril derivative, (H)BU[6] , lacking substituents on the ureidic nitrogen atoms, has been isolated and characterized. This macrocycle was prepared by the deprotection of bambusuril (PMB)BU[6] . (H)BU[6] is attractive for use as a starting compound for the preparation of other bambusuril derivatives, which was demonstrated via propargylation and the copper-catalyzed click reaction performed on the macrocycle.

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