Cu(I)-Catalyzed Intermolecular Diamination of Activated Terminal Olefins

This paper describes a novel intermolecular diamination process with CuCl as catalyst and di-tert-butylthiadiaziridine 1,1-dioxide as nitrogen source. A variety of activated terminal olefins can be effectively diaminated in good yields under mild reaction conditions.

Saved in:
Bibliographic Details
Published inOrganic letters Vol. 9; no. 24; pp. 4943 - 4945
Main Authors Zhao, Baoguo, Yuan, Weicheng, Du, Haifeng, Shi, Yian
Format Journal Article
LanguageEnglish
Published WASHINGTON American Chemical Society 22.11.2007
Amer Chemical Soc
Subjects
Online AccessGet full text

Cover

Loading…
Abstract This paper describes a novel intermolecular diamination process with CuCl as catalyst and di-tert-butylthiadiaziridine 1,1-dioxide as nitrogen source. A variety of activated terminal olefins can be effectively diaminated in good yields under mild reaction conditions.
AbstractList This paper describes a novel intermolecular diamination process with CuCl as catalyst and di-tert-butylthiadiaziridine 1,1-dioxide as nitrogen source. A variety of activated terminal olefins can be effectively diaminated in good yields under mild reaction conditions.
This paper describes a novel intermolecular diamination process with CuCl as catalyst and di-tert-butylthiadiaziridine 1,1-dioxide as nitrogen source. A variety of activated terminal olefins can be effectively diaminated in good yields under mild reaction conditions.This paper describes a novel intermolecular diamination process with CuCl as catalyst and di-tert-butylthiadiaziridine 1,1-dioxide as nitrogen source. A variety of activated terminal olefins can be effectively diaminated in good yields under mild reaction conditions.
Author Yuan, Weicheng
Zhao, Baoguo
Du, Haifeng
Shi, Yian
Author_xml – sequence: 1
  givenname: Baoguo
  surname: Zhao
  fullname: Zhao, Baoguo
– sequence: 2
  givenname: Weicheng
  surname: Yuan
  fullname: Yuan, Weicheng
– sequence: 3
  givenname: Haifeng
  surname: Du
  fullname: Du, Haifeng
– sequence: 4
  givenname: Yian
  surname: Shi
  fullname: Shi, Yian
BackLink https://www.ncbi.nlm.nih.gov/pubmed/17973481$$D View this record in MEDLINE/PubMed
BookMark eNqN0U1PHCEYB3DS2FRde-gXaObSRtOMPsAMMxzNaOsmJl7secKyDwmGAQuMjf30Zd3tNmk8lAsEfn_enmNy4INHQj5QOKfA6EVwHTAQNL0hR7RlvO6gZQf7sYBDcpzSAwAtM_IdOaSd7HjT0yNyM8yny7N6UFm551-4rpY-Y5yCQz07FasrqybrVbbBV8FUlzrbJ5WLuy-qLLjqzqGxPp2Qt0a5hO93_YJ8_3p9P9zUt3fflsPlba04yFxLJWDNWd8ip6zXUuqug55qA3plhGECWhRoVLtusG-ElD0wrholGFXUcM4X5PN238cYfsyY8jjZpNE55THMaRR9S-XmeQvycQfn1YTr8THaScXn8c_bC-i34Ceugknaote4ZwDAWpBdC5vWDDa_fMIQZp9L9Mv_R4s-22odQ0oRzd-7wLgp4LgvYLEX_1i9OzlHZd2riU_bhNJpfAhzLEVJr7jfN4ulAQ
CitedBy_id crossref_primary_10_1002_ange_200803184
crossref_primary_10_1038_s41596_018_0010_0
crossref_primary_10_1039_C5SC00897B
crossref_primary_10_1002_adsc_201700559
crossref_primary_10_1002_chin_200816046
crossref_primary_10_1016_j_tetlet_2010_01_114
crossref_primary_10_1038_s41467_019_13024_5
crossref_primary_10_1002_anie_202212292
crossref_primary_10_1002_anie_200804362
crossref_primary_10_1021_ol303469a
crossref_primary_10_1021_ol702974s
crossref_primary_10_1002_anie_201103077
crossref_primary_10_1021_ja2120629
crossref_primary_10_1002_ange_201003653
crossref_primary_10_1021_acs_orglett_4c00155
crossref_primary_10_1039_C9SC05335B
crossref_primary_10_1021_acs_joc_9b00936
crossref_primary_10_1039_D4OB00168K
crossref_primary_10_1002_ange_201209142
crossref_primary_10_1002_ange_202411992
crossref_primary_10_1016_j_tet_2010_04_054
crossref_primary_10_1021_ja906915w
crossref_primary_10_1021_jacs_1c00228
crossref_primary_10_1021_ja909459h
crossref_primary_10_1002_ange_201803668
crossref_primary_10_1002_ejoc_201301805
crossref_primary_10_1021_ol9000087
crossref_primary_10_1021_acs_orglett_2c02604
crossref_primary_10_1021_acs_orglett_5b00131
crossref_primary_10_1021_ol3034753
crossref_primary_10_1002_chem_201101703
crossref_primary_10_1002_slct_202004765
crossref_primary_10_1002_chem_200901199
crossref_primary_10_1351_PAC_CON_12_10_23
crossref_primary_10_1002_ange_201103077
crossref_primary_10_1021_om900329f
crossref_primary_10_1021_ja207691a
crossref_primary_10_1002_ange_200804362
crossref_primary_10_1002_anie_200803184
crossref_primary_10_1039_C6SC02231F
crossref_primary_10_1002_asia_200800148
crossref_primary_10_1002_chem_201600887
crossref_primary_10_1021_ja405394v
crossref_primary_10_1039_b716595c
crossref_primary_10_1039_C0CC04166A
crossref_primary_10_1002_anie_201003653
crossref_primary_10_1002_asia_200700373
crossref_primary_10_1021_om300840z
crossref_primary_10_1021_acs_joc_3c02690
crossref_primary_10_1039_c2sc20242e
crossref_primary_10_1002_anie_201209142
crossref_primary_10_1002_anie_201803668
crossref_primary_10_1002_anie_202411992
crossref_primary_10_1002_ange_202011996
crossref_primary_10_1021_ol102767j
crossref_primary_10_1021_ja506532h
crossref_primary_10_1021_ja803344v
crossref_primary_10_1039_b809633n
crossref_primary_10_1016_j_tet_2012_03_036
crossref_primary_10_1021_acs_orglett_1c01313
crossref_primary_10_1016_j_tetlet_2017_01_015
crossref_primary_10_1021_ol801605w
crossref_primary_10_1039_b719479j
crossref_primary_10_1021_cr400547x
crossref_primary_10_1002_adsc_201000813
crossref_primary_10_1002_ejoc_202300980
crossref_primary_10_1021_acs_orglett_2c03908
crossref_primary_10_1021_ol900808z
crossref_primary_10_1002_chem_201203832
crossref_primary_10_1021_jacs_7b06852
crossref_primary_10_1002_chem_201600393
crossref_primary_10_1021_jo202507d
crossref_primary_10_1021_ar500344t
crossref_primary_10_1002_anie_202011996
crossref_primary_10_1002_ange_202212292
crossref_primary_10_1038_s41467_023_37345_8
crossref_primary_10_1002_asia_201101025
crossref_primary_10_1039_D4QO01445F
crossref_primary_10_1002_chem_201402258
crossref_primary_10_1021_acs_joc_7b01313
crossref_primary_10_1038_nchem_256
crossref_primary_10_1039_C5CS00882D
crossref_primary_10_1021_acs_orglett_7b03401
crossref_primary_10_1039_C8OB02443J
crossref_primary_10_1021_ol302855z
crossref_primary_10_1021_cr500036t
crossref_primary_10_1021_jo302472w
crossref_primary_10_1039_D0CC01659D
crossref_primary_10_1021_acs_chemrev_8b00628
crossref_primary_10_1021_acs_joc_8b00933
crossref_primary_10_1021_cr050041j
Cites_doi 10.1021/ja055190y
10.1002/1521-3773(20011119)40:22<4277::AID-ANIE4277>3.0.CO;2-I
10.1021/ar9501434
10.1021/jo01260a005
10.1021/ja00039a091
10.1021/ja051181d
10.1021/ja072080d
10.1021/ol071105a
10.1021/ja00537a046
10.1002/(SICI)1521-3773(19981016)37:19<2580::AID-ANIE2580>3.0.CO;2-L
10.1021/cr00026a008
10.1021/ja053335v
10.1021/jo00323a021
10.1021/np9903292
10.1021/ol0706713
10.1021/ja0680562
10.1021/jo0200769
10.1111/j.1747-0285.2006.00347.x
10.1039/b107811a
10.1055/s-2006-9423
10.1039/b502150b
10.1016/j.bmcl.2004.12.018
10.1021/ol020002j
10.1021/ja0692581
ContentType Journal Article
Copyright Copyright © 2007 American Chemical Society
Copyright_xml – notice: Copyright © 2007 American Chemical Society
DBID AAYXX
CITATION
17B
1KM
1KN
BLEPL
DTL
EGQ
GAMXJ
CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1021/ol702061s
DatabaseName CrossRef
Web of Knowledge
Index Chemicus
Current Chemical Reactions
Web of Science Core Collection
Science Citation Index Expanded
Web of Science Primary (SCIE, SSCI & AHCI)
Web of Science - Science Citation Index Expanded - 2007
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle CrossRef
Web of Science
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList Web of Science

MEDLINE - Academic
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 1KN
  name: Current Chemical Reactions
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/woscc/search-with-editions?editions=WOS.CCR
  sourceTypes:
    Enrichment Source
    Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1523-7052
EndPage 4945
ExternalDocumentID 17973481
000250975000004
10_1021_ol702061s
a571861849
Genre Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID -
.K2
123
4.4
53G
55A
5VS
7~N
AABXI
ABFLS
ABMVS
ABPTK
ABUCX
ACGFS
ACS
AEESW
AENEX
AFEFF
ALMA_UNASSIGNED_HOLDINGS
AQSVZ
BAANH
CS3
DU5
DZ
EBS
ED
ED~
F5P
GNL
IH9
IHE
JG
JG~
K2
LG6
P2P
RNS
ROL
TN5
UI2
UNC
VF5
VG9
W1F
X
YNT
---
-DZ
-~X
AAHBH
AAYXX
ABBLG
ABJNI
ABLBI
ABQRX
ADHLV
AHGAQ
CITATION
CUPRZ
GGK
17B
1KM
1KN
BLEPL
DTL
GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED
GROUPED_WOS_WEB_OF_SCIENCE
CGR
CUY
CVF
ECM
EIF
NPM
7X8
ID FETCH-LOGICAL-a309t-9a60d3285e3128c99c77081cf0cbf6f2605e6efa5d4e846998023a4a621a1f333
IEDL.DBID ACS
ISICitedReferencesCount 90
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000250975000004
ISSN 1523-7060
IngestDate Fri Jul 11 15:43:05 EDT 2025
Mon Jul 21 06:03:57 EDT 2025
Fri Aug 29 15:55:37 EDT 2025
Tue Jun 17 07:27:39 EDT 2025
Tue Jul 01 02:12:27 EDT 2025
Thu Apr 24 23:01:16 EDT 2025
Thu Aug 27 13:42:00 EDT 2020
IsPeerReviewed true
IsScholarly true
Issue 24
Keywords ORGANIC-SYNTHESIS
PROMOTED INTRAMOLECULAR DIAMINATION
ELECTROPHILIC DIAMINATION
RADICAL CYCLIZATION
CONJUGATED DIENES
COMPLEXES
BISINDOLE ALKALOIDS
ALKENYL OXAZIRIDINES
VICINAL DIAMINATION
1,2-DIAMINATION
Language English
LinkModel DirectLink
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-a309t-9a60d3285e3128c99c77081cf0cbf6f2605e6efa5d4e846998023a4a621a1f333
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 17973481
PQID 68519797
PQPubID 23479
PageCount 3
ParticipantIDs webofscience_primary_000250975000004
crossref_primary_10_1021_ol702061s
webofscience_primary_000250975000004CitationCount
proquest_miscellaneous_68519797
crossref_citationtrail_10_1021_ol702061s
acs_journals_10_1021_ol702061s
pubmed_primary_17973481
ProviderPackageCode JG~
55A
AABXI
GNL
VF5
7~N
VG9
W1F
ACS
AEESW
AFEFF
.K2
ABMVS
ABUCX
IH9
BAANH
AQSVZ
ED~
UI2
CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2007-11-22
PublicationDateYYYYMMDD 2007-11-22
PublicationDate_xml – month: 11
  year: 2007
  text: 2007-11-22
  day: 22
PublicationDecade 2000
PublicationPlace WASHINGTON
PublicationPlace_xml – name: WASHINGTON
– name: United States
PublicationTitle Organic letters
PublicationTitleAbbrev ORG LETT
PublicationTitleAlternate Org. Lett
PublicationYear 2007
Publisher American Chemical Society
Amer Chemical Soc
Publisher_xml – name: American Chemical Society
– name: Amer Chemical Soc
References For (ol702061sb00018/ol702061sb00018_1) 1992; 114
For (ol702061sb00015/ol702061sb00015_1) 1994; 94
For (ol702061sb00001/ol702061sb00001_1) 1998; 37
Yuan W. (ol702061sb00009/ol702061sb00009_1) 2007; 9
Zabawa T. P. (ol702061sb00005/ol702061sb00005_2) 2007; 9
For (ol702061sb00008/ol702061sb00008_1) 2007; 129
For (ol702061sb00019/ol702061sb00019_1) 1992; 41
For (ol702061sb00016/ol702061sb00016_1) 1999; 32
Zabawa T. P. (ol702061sb00005/ol702061sb00005_1) 2005; 127
For (ol702061sb00011/ol702061sb00011_1) 1983
Du H. (ol702061sb00007/ol702061sb00007_1) 2007; 129
Prepared (ol702061sb00012/ol702061sb00012_1) 1981; 46
For (ol702061sb00020/ol702061sb00020_1) 2000; 63
Greene F. D. (ol702061sb00010/ol702061sb00010_1) 1969; 34
For (ol702061sb00002/ol702061sb00002_1) 1980; 102
Bar G. L. J. (ol702061sb00004/ol702061sb00004_1) 2005; 127
For (ol702061sb00003/ol702061sb00003_1) 2001; 40
Streuff J. (ol702061sb00006/ol702061sb00006_1) 2005; 127
For (ol702061sb00017/ol702061sb00017_1) 2001; 2
Clark, AJ (WOS:000173909300001) 2002; 31
Zabawa, TP (WOS:000231227400026) 2005; 127
Patten, TE (WOS:000083313200009) 1999; 32
LIPSHUTZ BH (WOS:000250975000004.24) 1992; 41
BECKER, PN (WOS:A1980KD12300046) 1980; 102
Kotti, SRSS (WOS:000236474300002) 2006; 67
Miyake, FY (WOS:000174441700019) 2002; 4
Black, DS (WOS:000238841100013) 2006
FRISTAD, WE (WOS:A1985ART2100049) 1985; 50
DU H (WOS:000250975000004.14) 2005; 129
TIMBERLAKE, JW (WOS:A1981LP46100021) 1981; 46
Wei, HX (WOS:000176600400020) 2002; 67
Aube, J (WOS:A1997YA13800004) 1997; 26
MORTENSEN MS (WOS:000250975000004.27) 2005; 18
HEINE HW (WOS:000250975000004.19) 1983
BACKVALL, JE (WOS:A1978EF41800023) 1978
Muniz, K (WOS:000229373600026) 2005
Masuyama, Y (WOS:000235414900003) 2006; 67
Muniz, K (WOS:000180860100013) 2003
GREENE, FD (WOS:A1969D898600005) 1969; 34
Zabawa, TP (WOS:000246190800049) 2007; 9
IQBAL, J (WOS:A1994NG03100008) 1994; 94
BARLUENGA, J (WOS:A1979HZ08000015) 1979
CHONG, AO (WOS:A1977DF06800039) 1977; 99
Streuff, J (WOS:000232780900029) 2005; 127
Kumar, V (WOS:000227135400044) 2005; 15
Bar, GLJ (WOS:000229244600023) 2005; 127
AUBE, J (WOS:A1992JA17100091) 1992; 114
Black, DS (WOS:000074905500052) 1998; 39
Guin, J (WOS:000245723800066) 2007; 129
GALL D (WOS:000250975000004.16) 1998; 37
ARANDA, VG (WOS:A1974T695200014) 1974
Yuan, WC (WOS:000247215700041) 2007; 9
STELLA L (WOS:000250975000004.31) 2001; 2
Du, HF (WOS:000247240500010) 2007; 129
Li, GG (WOS:000172329200036) 2001; 40
Casapullo, A (WOS:000086820700004) 2000; 63
References_xml – volume: 127
  start-page: 14586
  year: 2005
  ident: ol702061sb00006/ol702061sb00006_1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja055190y
– volume: 40
  start-page: 4277
  year: 2001
  ident: ol702061sb00003/ol702061sb00003_1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/1521-3773(20011119)40:22<4277::AID-ANIE4277>3.0.CO;2-I
– volume: 32
  start-page: 895
  year: 1999
  ident: ol702061sb00016/ol702061sb00016_1
  publication-title: Acc. Chem. Res.
  doi: 10.1021/ar9501434
– volume: 34
  start-page: 2254
  year: 1969
  ident: ol702061sb00010/ol702061sb00010_1
  publication-title: J. Org. Chem.
  doi: 10.1021/jo01260a005
– volume: 114
  start-page: 5466
  year: 1992
  ident: ol702061sb00018/ol702061sb00018_1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00039a091
– volume: 127
  start-page: 7308
  year: 2005
  ident: ol702061sb00004/ol702061sb00004_1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja051181d
– volume: 41
  start-page: 135
  year: 1992
  ident: ol702061sb00019/ol702061sb00019_1
  publication-title: Org. React.
– volume: 129
  start-page: 7496
  year: 2007
  ident: ol702061sb00008/ol702061sb00008_1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja072080d
– volume: 9
  start-page: 2589
  year: 2007
  ident: ol702061sb00009/ol702061sb00009_1
  publication-title: Org. Lett.
  doi: 10.1021/ol071105a
– volume: 2
  start-page: 407
  volume-title: L. In Radicals in Organic Synthesis
  year: 2001
  ident: ol702061sb00017/ol702061sb00017_1
– volume: 102
  start-page: 5676
  year: 1980
  ident: ol702061sb00002/ol702061sb00002_1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00537a046
– volume: 37
  start-page: 2580
  year: 1998
  ident: ol702061sb00001/ol702061sb00001_1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/(SICI)1521-3773(19981016)37:19<2580::AID-ANIE2580>3.0.CO;2-L
– volume: 94
  start-page: 519
  year: 1994
  ident: ol702061sb00015/ol702061sb00015_1
  publication-title: Chem. Rev.
  doi: 10.1021/cr00026a008
– volume: 127
  start-page: 11250
  year: 2005
  ident: ol702061sb00005/ol702061sb00005_1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja053335v
– volume: 46
  start-page: 2082
  year: 1981
  ident: ol702061sb00012/ol702061sb00012_1
  publication-title: J. Org. Chem.
  doi: 10.1021/jo00323a021
– volume: 63
  start-page: 447
  year: 2000
  ident: ol702061sb00020/ol702061sb00020_1
  publication-title: J. Nat. Prod.
  doi: 10.1021/np9903292
– volume: 9
  start-page: 2035
  year: 2007
  ident: ol702061sb00005/ol702061sb00005_2
  publication-title: Org. Lett.
  doi: 10.1021/ol0706713
– start-page: 547
  volume-title: H. W. In The Chemistry of Heterocyclic Compounds
  year: 1983
  ident: ol702061sb00011/ol702061sb00011_1
– volume: 129
  start-page: 762
  year: 2007
  ident: ol702061sb00007/ol702061sb00007_1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja0680562
– volume: 102
  start-page: 5676
  year: 1980
  ident: WOS:A1980KD12300046
  article-title: A NEW METHOD FOR 1,2-DIAMINATION OF ALKENES USING CYCLOPENTADIENYLNITROSYLCOBALT DIMER-NO-LIALH4
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 127
  start-page: 11250
  year: 2005
  ident: WOS:000231227400026
  article-title: Copper(II) acetate promoted intramolecular diamination of unactivated olefins
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja053335v
– volume: 129
  start-page: 762
  year: 2005
  ident: WOS:000250975000004.14
  publication-title: J AM CHEM SOC
– volume: 50
  start-page: 3647
  year: 1985
  ident: WOS:A1985ART2100049
  article-title: CONVERSION OF ALKENES TO 1,2-DIAZIDES AND 1,2-DIAMINES
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
– volume: 67
  start-page: 4777
  year: 2002
  ident: WOS:000176600400020
  article-title: Electrophilic diamination of alkenes by using FeCl3-PPh3 complex as the catalyst
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo0200769
– volume: 67
  start-page: 101
  year: 2006
  ident: WOS:000236474300002
  article-title: Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistry
  publication-title: CHEMICAL BIOLOGY & DRUG DESIGN
  doi: 10.1111/j.1747-0285.2006.00347.x
– start-page: 211
  year: 2003
  ident: WOS:000180860100013
  article-title: A first asymmetric diamination of olefins
  publication-title: SYNLETT
– volume: 9
  start-page: 2589
  year: 2007
  ident: WOS:000247215700041
  article-title: A mild Cu(I)-catalyzed regioselective diamination of conjugated dienes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol071105a
– volume: 18
  start-page: 555
  year: 2005
  ident: WOS:000250975000004.27
  publication-title: CHEMTRACTS ORG CHEM
– volume: 67
  start-page: 503
  year: 2006
  ident: WOS:000235414900003
  article-title: Tin(II) iodide-catalyzed selective aziridination or 1,2-diamination of alkenes with Chloramine-T
  publication-title: HETEROCYCLES
– start-page: 547
  year: 1983
  ident: WOS:000250975000004.19
  publication-title: CHEM HETEROCYCLIC CO
– volume: 114
  start-page: 5466
  year: 1992
  ident: WOS:A1992JA17100091
  article-title: NEW COPPER(I)-CATALYZED REACTIONS OF OXAZIRIDINES - STEREOCHEMICAL CONTROL OF PRODUCT DISTRIBUTION
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 129
  start-page: 7496
  year: 2007
  ident: WOS:000247240500010
  article-title: A Pd(0)-catalyzed diamination of terminal olefins at allylic and homoallylic carbons via formal C-H activation under solvent-free conditions
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja072080d
– volume: 31
  start-page: 1
  year: 2002
  ident: WOS:000173909300001
  article-title: Atom transfer radical cyclisation reactions mediated by copper complexes
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/b107811a
– volume: 26
  start-page: 269
  year: 1997
  ident: WOS:A1997YA13800004
  article-title: Oxaziridine rearrangements in asymmetric synthesis
  publication-title: CHEMICAL SOCIETY REVIEWS
– start-page: 962
  year: 1979
  ident: WOS:A1979HZ08000015
  article-title: MERCURY(II) OXIDE TETRAFLUOROBORIC ACID - NEW REAGENT IN ORGANIC-SYNTHESIS - CONVENIENT DIAMINATION OF OLEFINS
  publication-title: SYNTHESIS-STUTTGART
– volume: 34
  start-page: 2254
  year: 1969
  ident: WOS:A1969D898600005
  article-title: DIAZIRIDINONES (2,3-DIAZACYCLOPROPANONES) .2. SYNTHESIS, PROPERTIES, AND REACTIONS
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
– volume: 63
  start-page: 447
  year: 2000
  ident: WOS:000086820700004
  article-title: New bisindole alkaloids of the topsentin and hamacanthin classes from the Mediterranean marine sponge Rhaphisia lacazei
  publication-title: JOURNAL OF NATURAL PRODUCTS
– volume: 127
  start-page: 14586
  year: 2005
  ident: WOS:000232780900029
  article-title: Palladium(II)-catalyzed intramolecular diamination of unfunctionalized alkenes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja055190y
– volume: 32
  start-page: 895
  year: 1999
  ident: WOS:000083313200009
  article-title: Copper(I)-catalyzed atom transfer radical polymerization
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
– volume: 41
  start-page: 135
  year: 1992
  ident: WOS:000250975000004.24
  publication-title: ORG REACTIONS
– start-page: 1981
  year: 2006
  ident: WOS:000238841100013
  article-title: Synthesis and radical reactions of isomeric alkenyl oxaziridines
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-2006-9423
– start-page: 2729
  year: 2005
  ident: WOS:000229373600026
  article-title: Enantioselective catalytic diamination of alkenes with a bisimidoosmium oxidant
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b502150b
– volume: 99
  start-page: 3420
  year: 1977
  ident: WOS:A1977DF06800039
  article-title: SYNTHESIS OF DIOXOBIS(TERT-ALKYLIMIDO)OSMIUM(VIII) AND OXOTRIS(TERT-ALKYLIMIDO)OSMIUM(VIII) COMPLEXES - STEREOSPECIFIC VICINAL DIAMINATION OF OLEFINS
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 15
  start-page: 1091
  year: 2005
  ident: WOS:000227135400044
  article-title: Synthesis and evaluation of novel peripherally restrieted kappa-opioid receptor agonists
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  doi: 10.1016/j.bmcl.2004.12.018
– start-page: 504
  year: 1974
  ident: WOS:A1974T695200014
  article-title: ADDITION OF AROMATIC-AMINES TO ALKENES IN PRESENCE OF THALLIUM(III) ACETATE
  publication-title: SYNTHESIS-STUTTGART
– volume: 9
  start-page: 2035
  year: 2007
  ident: WOS:000246190800049
  article-title: Copper(II) carboxylate promoted intramolecular diamination of terminal alkenes: Improved reaction conditions and expanded substrate scope
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol0706713
– volume: 39
  start-page: 5853
  year: 1998
  ident: WOS:000074905500052
  article-title: Radical cyclisation from alkenyl oxaziridines
  publication-title: TETRAHEDRON LETTERS
– volume: 94
  start-page: 519
  year: 1994
  ident: WOS:A1994NG03100008
  article-title: TRANSITION METAL-PROMOTED FREE-RADICAL REACTIONS IN ORGANIC-SYNTHESIS - THE FORMATION OF CARBON-CARBON BONDS
  publication-title: CHEMICAL REVIEWS
– start-page: 163
  year: 1978
  ident: WOS:A1978EF41800023
  article-title: STEREOSPECIFIC PALLADIUM-PROMOTED VICINAL DIAMINATION OF OLEFINS
  publication-title: TETRAHEDRON LETTERS
– volume: 46
  start-page: 2082
  year: 1981
  ident: WOS:A1981LP46100021
  article-title: THIADIAZIRIDINE 1,1-DIOXIDES - SYNTHESIS AND CHEMISTRY
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
– volume: 4
  start-page: 941
  year: 2002
  ident: WOS:000174441700019
  article-title: Synthesis of marine sponge bisindole alkaloids dihydrohamacanthins
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol020002j
– volume: 127
  start-page: 7308
  year: 2005
  ident: WOS:000229244600023
  article-title: Pd(II)-catalyzed intermolecular 1,2-diamination of conjugated dienes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja051181d
– volume: 37
  start-page: 2580
  year: 1998
  ident: WOS:000250975000004.16
  publication-title: ANGEW CHEM INT EDIT
– volume: 40
  start-page: 4277
  year: 2001
  ident: WOS:000172329200036
  article-title: A novel electrophilic diamination reaction of alkenes
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
– volume: 129
  start-page: 4498
  year: 2007
  ident: WOS:000245723800066
  article-title: Radical transfer hydroamination with aminated cyclohexadienes using polarity reversal catalysis: Scope and limitations
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja0692581
– volume: 2
  start-page: 407
  year: 2001
  ident: WOS:000250975000004.31
  publication-title: RADICALS ORGANIC SYN
SSID ssj0011529
Score 2.2211199
Snippet This paper describes a novel intermolecular diamination process with CuCl as catalyst and di-tert-butylthiadiaziridine 1,1-dioxide as nitrogen source. A...
Source Web of Science
SourceID proquest
pubmed
webofscience
crossref
acs
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 4943
SubjectTerms Alkenes - chemistry
Amination
Catalysis
Chemistry
Chemistry, Organic
Copper - chemistry
Crystallography, X-Ray
Diamines - chemical synthesis
Diamines - chemistry
Models, Molecular
Molecular Structure
Physical Sciences
Science & Technology
Stereoisomerism
Title Cu(I)-Catalyzed Intermolecular Diamination of Activated Terminal Olefins
URI http://dx.doi.org/10.1021/ol702061s
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000250975000004
https://www.ncbi.nlm.nih.gov/pubmed/17973481
https://www.proquest.com/docview/68519797
Volume 9
WOS 000250975000004
WOSCitedRecordID wos000250975000004
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV25TsQwEB1xFNBwH-GMgAIKQ2zvOusSBdCCBBSARBc5ji0hliwi2QK-nnGOBcRytMkkUjx23vOM5w3AnsVFhDyeE8cmiFOUw_9gagnvaIloJqhhrsD58kp071oX9-37Mdj9IYPP6FG_FyKlETQfh0kmcPE6_hPdDFMFCECyFEVlnDgpmEY-6POjDnp0_hV6vvHJkdBTwszZLJw0xTrV6ZLHw0GRHOq379qNv33BHMzUNNM_rubFPIyZbAGmoqa72yJ0o8H--QGJXPTm9c2kfhkafGqa5fonruC7ihT6fesf67INGtrdVqdnev51z9iHLF-Cu7PT26hL6q4KRPFAFkQqEaScddqGIzZpKXUYIi_QNtCJFdbtb4wwVrXTlkFygtsxhHXVUoJRRS3nfBkmsn5mVsEXgVMPU4kNE9pKOkqmGgmTTGzgTmML4cEWDntcr4o8LhPejMbDAfFgv_FIrGtNctcaozfKdGdo-lwJcYwy2m7cGuN4utyHykx_kMei4yp0ZejBSuXtj5fgVVeN7MHeZ_cP7wclTZRhu9pPeUD_YxbVX-OUBYq1v8ZhHabLmDGlhLENmCheBmYTyU6RbJWT_R27ZPRD
linkProvider American Chemical Society
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3fb9MwED7BeBgvA8YG4UcXoT2MB484bp36sQpMLVvLA520t8hxbAlR0omkD-yv585J2gKV2Gtyseyznft85_sO4NThJkIcLxihCUaMcvgfLBwTQ6PQmkluY0pwns7k-Lr_-WZw09LkUC4MdqLCliofxN-wC_APy0WCyEby6iE8QhAS02oepV_XEQO0Q8pzo8aCESNMxyK0_SlZIFP9aYH-gZU7LZC3NhdPmrJFvp_-ksn381Wdn5u7vygc7zeQp3DQgs5w1KySZ_DAloewn3a13p7DOF2dTd6zlHw5v-5sEXpH4Y-udG74kdK_G79huHThyPiiaCg3b-7SLMIvC-u-ldURXF98mqdj1tZYYFpEqmZKy6gQ8XBgBVoqo5RJEkQJxkUmd9LRacdK6_Sg6FuEKng4QyOv-1rGXHMnhDiGvXJZ2pcQyoi4xHTukpz386FWhUH4pHIX0d1sKQPooT6ydo9UmQ9_xzxbKySAs25iMtMylFOhjMUu0Xdr0duGlmOX0Ek3uxnqkyIhurTLVZXJIeXrqiSAF82kbxrBp5SbHMDp9ipYv488aFTJoDldBcDvI5a2oyGegfrV__RwAvvj-fQqu5rMLl_DY-9N5pzF8RvYq3-u7FuEQXXe8-v_N7Jx_KQ
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1LT9wwEB5RkNpeKH3QpuURVRzowRDHu876uApdLbSFSgWJW-Q4toS6zaIme4Bf3xnnAW1XgmsysfyazDcezzcAew6VCHG8YIQmGDHK4X-wcEyMjEJrJrmNKcH526mcXgxOLoeXraNIuTDYiQpbqnwQn7T6unAtwwA_nM8SRDeSV09gjcJ1tKPH6Y8-aoC2SHl-1FgwYoXpmITuf0pWyFR_W6H_oOVSK-QtzuQFnPV99RdNfh4s6vzA3P5D4_j4wWzAegs-w3GzW17Cii1fwbO0q_n2GqbpYv_4E0vpTOfm1hahPzD81ZXQDY8oDbw5PwznLhwbXxwN5c6bOzWz8Gxm3VVZvYGLyefzdMraWgtMi0jVTGkZFSIeDa1Ai2WUMkmCaMG4yOROOvJ6rLROD4uBRciCThoaez3QMuaaOyHEJqyW89K-g1BGxCmmc5fkfJCPtCoMwiiVu4juaEsZwA7OSdbqSpX5MHjMs35CAtjvFiczLVM5FcyYLRP92IteN_Qcy4R2uxXOcD4pIqJLO19UmRxR3q5KAnjbLPxdI_iUcpQD2Lu_E_r3kQePKhk2XlYA_DFiaTsa4huo3z80D7vw9PvRJPt6fPrlAzz3h8qcszjegtX698JuIxqq8x2vAn8ADDf_Jw
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Cu%28I%29-catalyzed+intermolecular+diamination+of+activated+terminal+olefins&rft.jtitle=Organic+letters&rft.au=Zhao%2C+Baoguo&rft.au=Yuan%2C+Weicheng&rft.au=Du%2C+Haifeng&rft.au=Shi%2C+Yian&rft.date=2007-11-22&rft.pub=Amer+Chemical+Soc&rft.issn=1523-7060&rft.volume=9&rft.issue=24&rft.spage=4943&rft.epage=4945&rft_id=info:doi/10.1021%2Fol702061s&rft_id=info%3Apmid%2F17973481&rft.externalDBID=n%2Fa&rft.externalDocID=000250975000004
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1523-7060&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1523-7060&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1523-7060&client=summon