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

Keywords

Free radical cyclization
Gibberellin
Lactonization

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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 = "Amsterdam:Elsevier",

number = "5",

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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 - http://www.scopus.com/inward/record.url?scp=0035587922&partnerID=8YFLogxK

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

Keywords

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