Synthesis of Disubstituted Cucurbit[6]uril and Its Rotaxane Derivative

Hiroyuki Isobe; Sota Sato; Eiichi Nakamura

doi:10.1021/ol025749o

Synthesis of Disubstituted Cucurbit[6]uril and Its Rotaxane Derivative

Hiroyuki Isobe, Sota Sato, Eiichi Nakamura

Research output: Contribution to journal › Article › peer-review

142 Citations (Scopus)

Abstract

(Matrix Presented) Synthesis of diphenyl cucurbit[6]uril (CB[6]) has been achieved via co-oligomerization of diphenyl glycoluril and unsubstituted glycoluril. The unsymmetrically substituted CB[6], Ph₂CB[B], was further converted to a rotaxane incorporating bis(dinitrophenyl)spermine.

Original language	English
Pages (from-to)	1287-1289
Number of pages	3
Journal	Organic letters
Volume	4
Issue number	8
DOIs	https://doi.org/10.1021/ol025749o
Publication status	Published - 2002 Apr 18

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

Access to Document

10.1021/ol025749o

Cite this

@article{14ecdd8e581849fb8db4d467c5d606b2,

title = "Synthesis of Disubstituted Cucurbit[6]uril and Its Rotaxane Derivative",

abstract = "(Matrix Presented) Synthesis of diphenyl cucurbit[6]uril (CB[6]) has been achieved via co-oligomerization of diphenyl glycoluril and unsubstituted glycoluril. The unsymmetrically substituted CB[6], Ph2CB[B], was further converted to a rotaxane incorporating bis(dinitrophenyl)spermine.",

author = "Hiroyuki Isobe and Sota Sato and Eiichi Nakamura",

year = "2002",

month = apr,

day = "18",

doi = "10.1021/ol025749o",

language = "English",

volume = "4",

pages = "1287--1289",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "8",

}

TY - JOUR

T1 - Synthesis of Disubstituted Cucurbit[6]uril and Its Rotaxane Derivative

AU - Isobe, Hiroyuki

AU - Sato, Sota

AU - Nakamura, Eiichi

PY - 2002/4/18

Y1 - 2002/4/18

N2 - (Matrix Presented) Synthesis of diphenyl cucurbit[6]uril (CB[6]) has been achieved via co-oligomerization of diphenyl glycoluril and unsubstituted glycoluril. The unsymmetrically substituted CB[6], Ph2CB[B], was further converted to a rotaxane incorporating bis(dinitrophenyl)spermine.

AB - (Matrix Presented) Synthesis of diphenyl cucurbit[6]uril (CB[6]) has been achieved via co-oligomerization of diphenyl glycoluril and unsubstituted glycoluril. The unsymmetrically substituted CB[6], Ph2CB[B], was further converted to a rotaxane incorporating bis(dinitrophenyl)spermine.

UR - http://www.scopus.com/inward/record.url?scp=0037129379&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0037129379&partnerID=8YFLogxK

U2 - 10.1021/ol025749o

DO - 10.1021/ol025749o

M3 - Article

C2 - 11950344

AN - SCOPUS:0037129379

VL - 4

SP - 1287

EP - 1289

JO - Organic Letters

JF - Organic Letters

SN - 1523-7060

IS - 8

ER -

Synthesis of Disubstituted Cucurbit[6]uril and Its Rotaxane Derivative

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this