Iodoetherification of conformationally restricted dienyl alcohols: Unexpected formation of oxocenes by 8-endo-mode oxacyclizations

Kristen L. Stoltz; Andrea Nekane R. Alba; Frank E. McDonald; Marika B. Wieliczko; John Bacsa

doi:10.3987/COM-13-S(S)54

Iodoetherification of conformationally restricted dienyl alcohols: Unexpected formation of oxocenes by 8-endo-mode oxacyclizations

Kristen L. Stoltz
, Andrea Nekane R. Alba
, Frank E. McDonald
, Marika B. Wieliczko
, John Bacsa

Medicinal Chemistry

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

6 Scopus citations

Abstract

Iodine-promoted oxacyclizations of a family of conformationally restricted dienyl alcohols consistently afford oxocenes, arising from 8-endo-mode cyclizations.

Original language	English (US)
Pages (from-to)	1519-1526
Number of pages	8
Journal	Heterocycles
Volume	8
Issue number	2
DOIs	https://doi.org/10.3987/COM-13-S(S)54
State	Published - 2014

Bibliographical note

Funding Information:
This material is based upon work supported by the National Science Foundation under grant

Funding Information:
This material is based upon work supported by the National Science Foundation under grant CHE-1151304. A.N.R.A. thanks MICINN for supporting her research fellowship at Emory University.

Publisher Copyright:
© 2014 The Japan Institute of Heterocyclic Chemistry.

Publisher link

10.3987/COM-13-S(S)54

Find It

Find It at U of M Libraries

Cite this

@article{11ea6e4355ba44f683abe8659d784f56,

title = "Iodoetherification of conformationally restricted dienyl alcohols: Unexpected formation of oxocenes by 8-endo-mode oxacyclizations",

abstract = "Iodine-promoted oxacyclizations of a family of conformationally restricted dienyl alcohols consistently afford oxocenes, arising from 8-endo-mode cyclizations.",

author = "Stoltz, \{Kristen L.\} and Alba, \{Andrea Nekane R.\} and McDonald, \{Frank E.\} and Wieliczko, \{Marika B.\} and John Bacsa",

note = "Funding Information: This material is based upon work supported by the National Science Foundation under grant Funding Information: This material is based upon work supported by the National Science Foundation under grant CHE-1151304. A.N.R.A. thanks MICINN for supporting her research fellowship at Emory University. Publisher Copyright: {\textcopyright} 2014 The Japan Institute of Heterocyclic Chemistry.",

year = "2014",

doi = "10.3987/COM-13-S(S)54",

language = "English (US)",

volume = "8",

pages = "1519--1526",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

number = "2",

}

TY - JOUR

T1 - Iodoetherification of conformationally restricted dienyl alcohols

T2 - Unexpected formation of oxocenes by 8-endo-mode oxacyclizations

AU - Stoltz, Kristen L.

AU - Alba, Andrea Nekane R.

AU - McDonald, Frank E.

AU - Wieliczko, Marika B.

AU - Bacsa, John

N1 - Funding Information: This material is based upon work supported by the National Science Foundation under grant Funding Information: This material is based upon work supported by the National Science Foundation under grant CHE-1151304. A.N.R.A. thanks MICINN for supporting her research fellowship at Emory University. Publisher Copyright: © 2014 The Japan Institute of Heterocyclic Chemistry.

PY - 2014

Y1 - 2014

N2 - Iodine-promoted oxacyclizations of a family of conformationally restricted dienyl alcohols consistently afford oxocenes, arising from 8-endo-mode cyclizations.

AB - Iodine-promoted oxacyclizations of a family of conformationally restricted dienyl alcohols consistently afford oxocenes, arising from 8-endo-mode cyclizations.

UR - https://www.scopus.com/pages/publications/84986575827

UR - https://www.scopus.com/pages/publications/84986575827#tab=citedBy

U2 - 10.3987/COM-13-S(S)54

DO - 10.3987/COM-13-S(S)54

M3 - Article

AN - SCOPUS:84986575827

SN - 0385-5414

VL - 8

SP - 1519

EP - 1526

JO - Heterocycles

JF - Heterocycles

IS - 2

ER -

Iodoetherification of conformationally restricted dienyl alcohols: Unexpected formation of oxocenes by 8-endo-mode oxacyclizations

Abstract

Bibliographical note

Publisher link

Find It

Other files and links

Fingerprint

Cite this