Lariat ether alcohols based on dibenzo-16-crown-5

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

doi:10.1002/jhet.5570370554

Lariat ether alcohols based on dibenzo-16-crown-5

R. A. Bartsch, L. P. Bitalac, C. L. Cowey, S. Elshani, M. J. Goo, V. J. Huber, S. N. Ivy, Y. Jang, 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

12 Citations (Scopus)

Abstract

Synthetic routes to forty-four dibenzocrown ether alcohols are reported. The new crown ether compounds are based on a sym-dibenzo-16-crown-5 platform. Most have a hydroxy group and an alkyl, aryl, aralkyl, alkenyl, alkynyl, or perfluoroalkyl group on the central carbon of the three-carbon bridge. Others have substituted benzene rings and either a hydroxy or -O(CH₂)(n) OH group attached to the central carbon of the three-carbon bridge.

Original language	English
Pages (from-to)	1337-1350
Number of pages	14
Journal	Journal of Heterocyclic Chemistry
Volume	37
Issue number	5
DOIs	https://doi.org/10.1002/jhet.5570370554
Publication status	Published - 2000
Externally published	Yes

ASJC Scopus subject areas

Organic Chemistry

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title = "Lariat ether alcohols based on dibenzo-16-crown-5",

abstract = "Synthetic routes to forty-four dibenzocrown ether alcohols are reported. The new crown ether compounds are based on a sym-dibenzo-16-crown-5 platform. Most have a hydroxy group and an alkyl, aryl, aralkyl, alkenyl, alkynyl, or perfluoroalkyl group on the central carbon of the three-carbon bridge. Others have substituted benzene rings and either a hydroxy or -O(CH2)(n) OH group attached to the central carbon of the three-carbon bridge.",

author = "Bartsch, {R. A.} and Bitalac, {L. P.} and Cowey, {C. L.} and S. Elshani and Goo, {M. J.} and Huber, {V. J.} and Ivy, {S. N.} and Y. Jang 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 = "2000",

doi = "10.1002/jhet.5570370554",

language = "English",

volume = "37",

pages = "1337--1350",

journal = "Journal of Heterocyclic Chemistry",

issn = "0022-152X",

publisher = "Heterocorporation",

number = "5",

}

TY - JOUR

T1 - Lariat ether alcohols based on dibenzo-16-crown-5

AU - Bartsch, R. A.

AU - Bitalac, L. P.

AU - Cowey, C. L.

AU - Elshani, S.

AU - Goo, M. J.

AU - Huber, V. J.

AU - Ivy, S. N.

AU - Jang, Y.

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 - 2000

Y1 - 2000

N2 - Synthetic routes to forty-four dibenzocrown ether alcohols are reported. The new crown ether compounds are based on a sym-dibenzo-16-crown-5 platform. Most have a hydroxy group and an alkyl, aryl, aralkyl, alkenyl, alkynyl, or perfluoroalkyl group on the central carbon of the three-carbon bridge. Others have substituted benzene rings and either a hydroxy or -O(CH2)(n) OH group attached to the central carbon of the three-carbon bridge.

AB - Synthetic routes to forty-four dibenzocrown ether alcohols are reported. The new crown ether compounds are based on a sym-dibenzo-16-crown-5 platform. Most have a hydroxy group and an alkyl, aryl, aralkyl, alkenyl, alkynyl, or perfluoroalkyl group on the central carbon of the three-carbon bridge. Others have substituted benzene rings and either a hydroxy or -O(CH2)(n) OH group attached to the central carbon of the three-carbon bridge.

UR - http://www.scopus.com/inward/record.url?scp=0033767698&partnerID=8YFLogxK

U2 - 10.1002/jhet.5570370554

DO - 10.1002/jhet.5570370554

M3 - Article

AN - SCOPUS:0033767698

SN - 0022-152X

VL - 37

SP - 1337

EP - 1350

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

IS - 5

ER -

Lariat ether alcohols based on dibenzo-16-crown-5

Abstract

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