1997
DOI: 10.1039/a702995k
|View full text |Cite
|
Sign up to set email alerts
|

A Cage Compound containing Four Thiophene Rings: Synthesis and Structural Conversion by Desulfurization

Abstract: A novel macrocyclic cage compound with four thiophene rings was synthesized following a one-step procedure and then structurally converted by disulfurization.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

1998
1998
2008
2008

Publication Types

Select...
3
2

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(1 citation statement)
references
References 5 publications
0
1
0
Order By: Relevance
“…Unfortunately, this synthetic approach is not useful for the preparation of small supercryptands with aliphatic connecting groups because small five-or six-membered rings, such as morpholine or piperazine, will preferentially form. Some aliphatic connecting group-containing supercryptands shown in Scheme 33 have been prepared, but in small yields [95][96][97]. However, reactions of the appropriate starting materials do not always give the desired supercryptands but often lead to other macrocyclic compounds as shown in Scheme 34 [96].…”
Section: Macrocyclic Compounds Formed By Twelve New Bondsmentioning
confidence: 99%
“…Unfortunately, this synthetic approach is not useful for the preparation of small supercryptands with aliphatic connecting groups because small five-or six-membered rings, such as morpholine or piperazine, will preferentially form. Some aliphatic connecting group-containing supercryptands shown in Scheme 33 have been prepared, but in small yields [95][96][97]. However, reactions of the appropriate starting materials do not always give the desired supercryptands but often lead to other macrocyclic compounds as shown in Scheme 34 [96].…”
Section: Macrocyclic Compounds Formed By Twelve New Bondsmentioning
confidence: 99%