schliessen

Filtern

 

Bibliotheken

Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles.

Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles has been developed via cooperative catalysis of a chiral N,N'-dioxide-Sc(OTf)(3) complex and a Brønsted base. Utilizing readily available N-(phenylthio)phthalimide as the sulfur source, a wide range of optically active 3-pheny... Full description

Journal Title: Organic letters June 1, 2012, Vol.14(11), pp.2726-2729
Main Author: Cai, Yunfei
Other Authors: Li, Jun , Chen, Weiliang , Xie, Mingsheng , Liu, Xiaohua , Lin, Lili , Feng, Xiaoming
Format: Electronic Article Electronic Article
Language: English
Subjects:
ID: E-ISSN: 1523-7052 ; DOI: 10.1021/ol3009446
Link: http://search.proquest.com/docview/1018347245/?pq-origsite=primo
Zum Text:
SendSend as email Add to Book BagAdd to Book Bag
Staff View
recordid: proquest1018347245
title: Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles.
format: Article
creator:
  • Cai, Yunfei
  • Li, Jun
  • Chen, Weiliang
  • Xie, Mingsheng
  • Liu, Xiaohua
  • Lin, Lili
  • Feng, Xiaoming
subjects:
  • Catalysis–Chemical Synthesis
  • Combinatorial Chemistry Techniques–Chemistry
  • Indoles–Chemistry
  • Mesylates–Chemistry
  • Molecular Structure–Chemistry
  • Oxindoles–Chemistry
  • Scandium–Chemistry
  • Stereoisomerism–Chemistry
  • Sulfhydryl Compounds–Chemistry
  • Indoles
  • Mesylates
  • Oxindoles
  • Sulfhydryl Compounds
  • Scandium Triflate
  • 2-Oxindole
  • Scandium
ispartof: Organic letters, June 1, 2012, Vol.14(11), pp.2726-2729
description: Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles has been developed via cooperative catalysis of a chiral N,N'-dioxide-Sc(OTf)(3) complex and a Brønsted base. Utilizing readily available N-(phenylthio)phthalimide as the sulfur source, a wide range of optically active 3-phenylthiooxindoles were obtained in excellent yields with excellent enantioselectivities under mild reaction conditions.
language: eng
source:
identifier: E-ISSN: 1523-7052 ; DOI: 10.1021/ol3009446
fulltext: fulltext
issn:
  • 15237052
  • 1523-7052
url: Link


@attributes
ID1600446512
RANK0.07
NO1
SEARCH_ENGINEprimo_central_multiple_fe
SEARCH_ENGINE_TYPEPrimo Central Search Engine
LOCALfalse
PrimoNMBib
record
control
sourcerecordid1018347245
sourceidproquest
recordidTN_proquest1018347245
sourcesystemPC
pqid1018347245
display
typearticle
titleCatalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles.
creatorCai, Yunfei ; Li, Jun ; Chen, Weiliang ; Xie, Mingsheng ; Liu, Xiaohua ; Lin, Lili ; Feng, Xiaoming
contributorCai, Yunfei (correspondence author) ; Cai, Yunfei (record owner)
ispartofOrganic letters, June 1, 2012, Vol.14(11), pp.2726-2729
identifierE-ISSN: 1523-7052 ; DOI: 10.1021/ol3009446
subjectCatalysis–Chemical Synthesis ; Combinatorial Chemistry Techniques–Chemistry ; Indoles–Chemistry ; Mesylates–Chemistry ; Molecular Structure–Chemistry ; Oxindoles–Chemistry ; Scandium–Chemistry ; Stereoisomerism–Chemistry ; Sulfhydryl Compounds–Chemistry ; Indoles ; Mesylates ; Oxindoles ; Sulfhydryl Compounds ; Scandium Triflate ; 2-Oxindole ; Scandium
languageeng
source
descriptionCatalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles has been developed via cooperative catalysis of a chiral N,N'-dioxide-Sc(OTf)(3) complex and a Brønsted base. Utilizing readily available N-(phenylthio)phthalimide as the sulfur source, a wide range of optically active 3-phenylthiooxindoles were obtained in excellent yields with excellent enantioselectivities under mild reaction conditions.
version3
lds50peer_reviewed
links
openurl$$Topenurl_article
openurlfulltext$$Topenurlfull_article
backlink$$Uhttp://search.proquest.com/docview/1018347245/?pq-origsite=primo$$EView_record_in_ProQuest_(subscribers_only)
search
creatorcontrib
0Cai, Yunfei
1Li, Jun
2Chen, Weiliang
3Xie, Mingsheng
4Liu, Xiaohua
5Lin, Lili
6Feng, Xiaoming
titleCatalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles.
subject
0Catalysis–Chemical Synthesis
1Combinatorial Chemistry Techniques–Chemistry
2Indoles–Chemistry
3Mesylates–Chemistry
4Molecular Structure–Chemistry
5Oxindoles–Chemistry
6Scandium–Chemistry
7Stereoisomerism–Chemistry
8Sulfhydryl Compounds–Chemistry
9Indoles
10Mesylates
11Oxindoles
12Sulfhydryl Compounds
13Scandium Triflate
142-Oxindole
15Scandium
general
0English
110.1021/ol3009446
2MEDLINE (ProQuest)
3ProQuest Biological Science Collection
4ProQuest Natural Science Collection
5ProQuest SciTech Collection
6Biological Science Database
7Natural Science Collection
8SciTech Premium Collection
9Health Research Premium Collection
10Health Research Premium Collection (Alumni edition)
11Biological Science Index (ProQuest)
sourceidproquest
recordidproquest1018347245
issn
015237052
11523-7052
rsrctypearticle
creationdate2012
addtitleOrganic letters
searchscope
01007527
11007944
21009130
310000004
410000038
510000050
610000120
710000159
810000238
910000253
1010000260
1110000270
1210000271
1310000302
1410000350
15proquest
scope
01007527
11007944
21009130
310000004
410000038
510000050
610000120
710000159
810000238
910000253
1010000260
1110000270
1210000271
1310000302
1410000350
15proquest
lsr43
01007527false
11007944false
21009130false
310000004false
410000038false
510000050false
610000120false
710000159false
810000238false
910000253false
1010000260false
1110000270false
1210000271false
1310000302false
1410000350false
contributorCai, Yunfei
startdate20120601
enddate20120601
citationpf 2726 pt 2729 vol 14 issue 11
lsr30VSR-Enriched:[issn, description, pqid]
sort
titleCatalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles.
authorCai, Yunfei ; Li, Jun ; Chen, Weiliang ; Xie, Mingsheng ; Liu, Xiaohua ; Lin, Lili ; Feng, Xiaoming
creationdate20120601
lso0120120601
facets
frbrgroupid7155114579177552863
frbrtype5
newrecords20181218
languageeng
creationdate2012
topic
0Catalysis–Chemical Synthesis
1Combinatorial Chemistry Techniques–Chemistry
2Indoles–Chemistry
3Mesylates–Chemistry
4Molecular Structure–Chemistry
5Oxindoles–Chemistry
6Scandium–Chemistry
7Stereoisomerism–Chemistry
8Sulfhydryl Compounds–Chemistry
9Indoles
10Mesylates
11Oxindoles
12Sulfhydryl Compounds
13Scandium Triflate
142-Oxindole
15Scandium
collection
0MEDLINE (ProQuest)
1ProQuest Biological Science Collection
2ProQuest Natural Science Collection
3ProQuest SciTech Collection
4Biological Science Database
5Natural Science Collection
6SciTech Premium Collection
7Health Research Premium Collection
8Health Research Premium Collection (Alumni edition)
9Biological Science Index (ProQuest)
prefilterarticles
rsrctypearticles
creatorcontrib
0Cai, Yunfei
1Li, Jun
2Chen, Weiliang
3Xie, Mingsheng
4Liu, Xiaohua
5Lin, Lili
6Feng, Xiaoming
jtitleOrganic letters
toplevelpeer_reviewed
delivery
delcategoryRemote Search Resource
fulltextfulltext
addata
aulast
0Cai
1Li
2Chen
3Xie
4Liu
5Lin
6Feng
aufirst
0Yunfei
1Jun
2Weiliang
3Mingsheng
4Xiaohua
5Lili
6Xiaoming
au
0Cai, Yunfei
1Li, Jun
2Chen, Weiliang
3Xie, Mingsheng
4Liu, Xiaohua
5Lin, Lili
6Feng, Xiaoming
addauCai, Yunfei
atitleCatalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles.
jtitleOrganic letters
risdate20120601
volume14
issue11
spage2726
epage2729
pages2726-2729
eissn1523-7052
formatjournal
genrearticle
ristypeJOUR
doi10.1021/ol3009446
urlhttp://search.proquest.com/docview/1018347245/
issn15237060
date2012-06-01