Synthesis of lariat ether carboxylic acids based on dibenzo- 16-crown-5

R. A. Bartsch; C. L. Cowey; S. Elshani; M. J. Goo; V. J. Huber; S. N. Ivy; R. J. Johnson; J. S. Kim; E. Luboch; J. A. McDonough; M. J. Pugia; B. Son; Q. Zhao

doi:10.1002/jhet.5570380201

Synthesis of lariat ether carboxylic acids based on dibenzo- 16-crown-5

R. A. Bartsch, C. L. Cowey, S. Elshani, M. J. Goo, V. J. Huber, S. N. Ivy, R. J. Johnson, J. S. Kim, E. Luboch, J. A. McDonough, M. J. Pugia, B. Son, Q. Zhao

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

10 Citations (Scopus)

Abstract

Synthetic routes to forty-seven dibenzo-16-crown-5 compounds with pendant carboxylic acid groups are reported. When taken together with previously described lariat ether carboxylic acids, these new compounds provide several series with systematic structural variations including changes in the identity and attachment site(s) of one or more lipophilic groups and the length of the spacer that connects the carboxylic acid group to the polyether framework.

Original language	English
Pages (from-to)	311-331
Number of pages	21
Journal	Journal of Heterocyclic Chemistry
Volume	38
Issue number	2
DOIs	https://doi.org/10.1002/jhet.5570380201
Publication status	Published - 2001
Externally published	Yes

ASJC Scopus subject areas

Organic Chemistry

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title = "Synthesis of lariat ether carboxylic acids based on dibenzo- 16-crown-5",

abstract = "Synthetic routes to forty-seven dibenzo-16-crown-5 compounds with pendant carboxylic acid groups are reported. When taken together with previously described lariat ether carboxylic acids, these new compounds provide several series with systematic structural variations including changes in the identity and attachment site(s) of one or more lipophilic groups and the length of the spacer that connects the carboxylic acid group to the polyether framework.",

author = "Bartsch, {R. A.} and Cowey, {C. L.} and S. Elshani and Goo, {M. J.} and Huber, {V. J.} and Ivy, {S. N.} and Johnson, {R. J.} and Kim, {J. S.} and E. Luboch and McDonough, {J. A.} and Pugia, {M. J.} and B. Son and Q. Zhao",

year = "2001",

doi = "10.1002/jhet.5570380201",

language = "English",

volume = "38",

pages = "311--331",

journal = "Journal of Heterocyclic Chemistry",

issn = "0022-152X",

publisher = "Heterocorporation",

number = "2",

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TY - JOUR

T1 - Synthesis of lariat ether carboxylic acids based on dibenzo- 16-crown-5

AU - Bartsch, R. A.

AU - Cowey, C. L.

AU - Elshani, S.

AU - Goo, M. J.

AU - Huber, V. J.

AU - Ivy, S. N.

AU - Johnson, R. J.

AU - Kim, J. S.

AU - Luboch, E.

AU - McDonough, J. A.

AU - Pugia, M. J.

AU - Son, B.

AU - Zhao, Q.

PY - 2001

Y1 - 2001

N2 - Synthetic routes to forty-seven dibenzo-16-crown-5 compounds with pendant carboxylic acid groups are reported. When taken together with previously described lariat ether carboxylic acids, these new compounds provide several series with systematic structural variations including changes in the identity and attachment site(s) of one or more lipophilic groups and the length of the spacer that connects the carboxylic acid group to the polyether framework.

AB - Synthetic routes to forty-seven dibenzo-16-crown-5 compounds with pendant carboxylic acid groups are reported. When taken together with previously described lariat ether carboxylic acids, these new compounds provide several series with systematic structural variations including changes in the identity and attachment site(s) of one or more lipophilic groups and the length of the spacer that connects the carboxylic acid group to the polyether framework.

UR - http://www.scopus.com/inward/record.url?scp=0035052229&partnerID=8YFLogxK

U2 - 10.1002/jhet.5570380201

DO - 10.1002/jhet.5570380201

M3 - Article

AN - SCOPUS:0035052229

SN - 0022-152X

VL - 38

SP - 311

EP - 331

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

IS - 2

ER -

Synthesis of lariat ether carboxylic acids based on dibenzo- 16-crown-5

Abstract

ASJC Scopus subject areas

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