Přehled o publikaci
2023
Synthesis of Enantiomerically Pure Bambus[6]urils Utilizing Orthogonal Protection of Glycolurils
SLÁVIK, Petr; Jacopo TORRISI; Pia Yasmine JURČEK; Jan SOKOLOV; Vladimír ŠINDELÁŘ et. al.Basic information
Original name
Synthesis of Enantiomerically Pure Bambus[6]urils Utilizing Orthogonal Protection of Glycolurils
Authors
SLÁVIK, Petr (203 Czech Republic, belonging to the institution); Jacopo TORRISI (380 Italy, belonging to the institution); Pia Yasmine JURČEK (246 Finland, belonging to the institution); Jan SOKOLOV (203 Czech Republic, belonging to the institution) and Vladimír ŠINDELÁŘ (203 Czech Republic, guarantor, belonging to the institution)
Edition
Journal of Organic Chemistry, WASHINGTON, AMER CHEMICAL SOC, 2023, 0022-3263
Other information
Language
English
Type of outcome
Article in a journal
Country of publisher
United States of America
Confidentiality degree
is not subject to a state or trade secret
References:
RIV identification code
RIV/00216224:14310/23:00131646
Organization
Přírodovědecká fakulta – Repository – Repository
UT WoS
001039563400001
EID Scopus
2-s2.0-85167821150
Keywords in English
FLUORINATED BAMBUSURILS; DEPROTECTION; RECOGNITION; CUCURBITURIL; CATALYSTS; BINDING; WATER; ALKYL
Links
EF17_043/0009632, research and development project. GA23-05271S, research and development project. LM2018121, research and development project. MUNI/A/1209/2022, interní kód Repo. 857560, interní kód Repo. CIISB II, large research infrastructures.
Changed: 10/10/2024 00:50, RNDr. Daniel Jakubík
Abstract
V originále
amp; PRIME;-disubstitutedglycoluril enantiomers on a multigramscale using orthogonal protection is reported. The use of these glycolurilsis demonstrated in the synthesis of enantiomerically pure bambus[6]urilmacrocycles. Moreover, the deprotection of (S)-1-phenylethylsubstituents on the macrocycle was achieved, opening access to variouschiral bambus[6]urils via post-macrocyclization modificationstrategy.
