Stereoselective Functionalization at C-2 and C-3 of the Gibberellin via an Intramolecular Free Radical Cyclization Approach

An Qi Chen; Christine L. Willis

Stereoselective Functionalization at C-2 and C-3 of the Gibberellin via an Intramolecular Free Radical Cyclization Approach

An Qi Chen^*, Christine L. Willis

^*Corresponding author for this work

School of Chemistry

Research output: Contribution to journal › Article (Academic Journal) › peer-review

1 Citation (Scopus)

Abstract

Stereoselective functionalization at C-2 and C-3 of the gibberellin skeleton was achieved via an intramolecular free radical cyclization approach using a tethered C-19 halomethyl ester as the radical precursor.

Original language	English
Pages (from-to)	397-398
Number of pages	2
Journal	Chinese Chemical Letters
Volume	12
Issue number	5
Publication status	Published - May 2001

Research Groups and Themes

Organic & Biological

Keywords

Free radical cyclization
Gibberellin
Lactonization

Handle.net

Persistent link

Cite this

@article{6a04d2886abb4b419b9e1d26fa959ce8,

title = "Stereoselective Functionalization at C-2 and C-3 of the Gibberellin via an Intramolecular Free Radical Cyclization Approach",

abstract = "Stereoselective functionalization at C-2 and C-3 of the gibberellin skeleton was achieved via an intramolecular free radical cyclization approach using a tethered C-19 halomethyl ester as the radical precursor.",

keywords = "Free radical cyclization, Gibberellin, Lactonization",

author = "Chen, \{An Qi\} and Willis, \{Christine L.\}",

year = "2001",

month = may,

language = "English",

volume = "12",

pages = "397--398",

journal = "Chinese Chemical Letters",

issn = "1001-8417",

publisher = "Elsevier B.V.",

number = "5",

}

TY - JOUR

T1 - Stereoselective Functionalization at C-2 and C-3 of the Gibberellin via an Intramolecular Free Radical Cyclization Approach

AU - Chen, An Qi

AU - Willis, Christine L.

PY - 2001/5

Y1 - 2001/5

N2 - Stereoselective functionalization at C-2 and C-3 of the gibberellin skeleton was achieved via an intramolecular free radical cyclization approach using a tethered C-19 halomethyl ester as the radical precursor.

AB - Stereoselective functionalization at C-2 and C-3 of the gibberellin skeleton was achieved via an intramolecular free radical cyclization approach using a tethered C-19 halomethyl ester as the radical precursor.

KW - Free radical cyclization

KW - Gibberellin

KW - Lactonization

UR - https://www.scopus.com/pages/publications/0035587922

M3 - Article (Academic Journal)

AN - SCOPUS:0035587922

SN - 1001-8417

VL - 12

SP - 397

EP - 398

JO - Chinese Chemical Letters

JF - Chinese Chemical Letters

IS - 5

ER -

Stereoselective Functionalization at C-2 and C-3 of the Gibberellin via an Intramolecular Free Radical Cyclization Approach

Abstract

Research Groups and Themes

Keywords

Handle.net

Other files and links

Fingerprint

Cite this