Zhang, H and Jeon, KO and Hay, EB and Geib, SJ and Curran, DP and Laporte, MG
(2014)
Radical [3 + 2]-annulation of divinylcyclopropanes: Rapid synthesis of complex meloscine analogs.
Organic Letters, 16 (1).
94 - 97.
ISSN 1523-7060
![[img]](http://d-scholarship-dev.library.pitt.edu/style/images/fileicons/text_plain.png) |
Plain Text (licence)
Available under License : See the attached license file.
Download (1kB)
|
Abstract
A radical [3 + 2]-divinylcyclopropane annulation cascade has been extended to encompass five D-ring variants of the meloscine/epimeloscine core structure. Representative ABCD tetracyclic intermediates were further elaborated with novel substituted E-rings through subsequent transformations of advanced intermediates that provided opportunities for late-stage variation of the B-ring (lactam) N-substituents which were also developed. © 2013 American Chemical Society.
Share
Citation/Export: |
|
Social Networking: |
|
Details
Item Type: |
Article
|
Status: |
Published |
Creators/Authors: |
|
Date: |
3 January 2014 |
Date Type: |
Publication |
Journal or Publication Title: |
Organic Letters |
Volume: |
16 |
Number: |
1 |
Page Range: |
94 - 97 |
DOI or Unique Handle: |
10.1021/ol403078e |
Schools and Programs: |
Dietrich School of Arts and Sciences > Chemistry |
Refereed: |
Yes |
ISSN: |
1523-7060 |
MeSH Headings: |
Cyclization; Cyclopropanes--chemical synthesis; Cyclopropanes--chemistry; Models, Molecular; Molecular Structure; Polycyclic Compounds--chemical synthesis; Polycyclic Compounds--chemistry; Quinolines--chemical synthesis; Quinolines--chemistry |
Other ID: |
NLM NIHMS547519, NLM PMC3910537 |
PubMed Central ID: |
PMC3910537 |
PubMed ID: |
24313360 |
Date Deposited: |
23 Jul 2015 14:36 |
Last Modified: |
02 Feb 2019 15:57 |
URI: |
http://d-scholarship-dev.library.pitt.edu/id/eprint/25736 |
Metrics
Monthly Views for the past 3 years
Plum Analytics
Altmetric.com
Actions (login required)
![View Item View Item](/style/images/action_view.png) |
View Item |