ChemInform Abstract: Chemoselective Amide Formation Using O-(4-Nitrophenyl)hydroxylamines and Pyruvic Acid Derivatives

The reaction allows an efficient access to amides.

Saved in:
Bibliographic Details
Published inChemInform Vol. 44; no. 23; p. no
Main Authors Kumar, Sonali, Sharma, Rashi, Garcia, Megan, Kamel, Joseph, McCarthy, Caroline, Muth, Aaron, Phanstiel, Otto IV
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 04.06.2013
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
Subjects
carboxylic amides (acyclic compounds)
Online AccessGet full text

Cover

Abstract The reaction allows an efficient access to amides.
AbstractList The reaction allows an efficient access to amides.
Abstract The reaction allows an efficient access to amides.
The reaction allows an efficient access to amides. [PUBLICATION ABSTRACT]
Author Sharma, Rashi
McCarthy, Caroline
Garcia, Megan
Muth, Aaron
Kumar, Sonali
Phanstiel, Otto IV
Kamel, Joseph
Author_xml – sequence: 1
  givenname: Sonali
  surname: Kumar
  fullname: Kumar, Sonali
  organization: Dep. Med. Educ., Univ. Cent. Fla., Orlando, FL 32816, USA
– sequence: 2
  givenname: Rashi
  surname: Sharma
  fullname: Sharma, Rashi
  organization: Dep. Med. Educ., Univ. Cent. Fla., Orlando, FL 32816, USA
– sequence: 3
  givenname: Megan
  surname: Garcia
  fullname: Garcia, Megan
  organization: Dep. Med. Educ., Univ. Cent. Fla., Orlando, FL 32816, USA
– sequence: 4
  givenname: Joseph
  surname: Kamel
  fullname: Kamel, Joseph
  organization: Dep. Med. Educ., Univ. Cent. Fla., Orlando, FL 32816, USA
– sequence: 5
  givenname: Caroline
  surname: McCarthy
  fullname: McCarthy, Caroline
  organization: Dep. Med. Educ., Univ. Cent. Fla., Orlando, FL 32816, USA
– sequence: 6
  givenname: Aaron
  surname: Muth
  fullname: Muth, Aaron
  organization: Dep. Med. Educ., Univ. Cent. Fla., Orlando, FL 32816, USA
– sequence: 7
  givenname: Otto IV
  surname: Phanstiel
  fullname: Phanstiel, Otto IV
  organization: Dep. Med. Educ., Univ. Cent. Fla., Orlando, FL 32816, USA
BookMark eNqFkEFPGzEQRq2KSg20154t9QKHDR57185yCwFCpDT0UNTeLLOebQy7drA3Kfvvu1EQ4tbTSKP3vtF8x-TIB4-EfAU2Bsb4ebV2fswZCC6YKD-QERScZ1xKdURGrBSQqaJUn8hxSo8DL9SEj8hutsZ24esQWzp9SF00VXdB98uQsMGqczuk09ZZpDcDYzoXPL1Pzv-hd9lpnq1cF8Nmjb5vzta9jeGlb0zrPCZqvKU_-rjduYpOK2fpFUa3M_vE9Jl8rE2T8MvrPCH3N9c_Z7fZ8m6-mE2XWQVFUWalkVYpU1sA-yCZwXx4o1aVQUAhrZhICVByxtEgQ-DcoK3ziZ3kNSsYGHFCvh1yNzE8bzF1-jFsox9OahAFSCZ4DgM1PlBVDClFrPUmutbEXgPT-271vlv91u0glAfhr2uw_w-tZ7eL1Xs3O7gudfjy5pr4pKUSqtC_VnN9JYrL-e_ld63EPy2Uj9A
Cites_doi 10.1021/jo302175g
ContentType Journal Article
Copyright 2013 WILEY‐VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany
2013 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany
Copyright_xml – notice: 2013 WILEY‐VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany
– notice: 2013 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany
DBID BSCLL
AAYXX
CITATION
DOI 10.1002/chin.201323039
DatabaseName Istex
CrossRef
DatabaseTitle CrossRef
DatabaseTitleList
CrossRef
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1522-2667
EndPage no
ExternalDocumentID 2971228161
10_1002_chin_201323039
CHIN201323039
ark_67375_WNG_D35BGXLM_7
Genre article
GroupedDBID 05W
1L6
1OC
29B
3WU
4.4
50Y
5GY
66C
8-0
8-1
8UM
A00
AAESR
AAZKR
ABDBF
ABIJN
ABJNI
ACBWZ
ACGFS
ACIWK
ACXQS
AEUCX
AEUQT
AFBPY
AFZJQ
ALMA_UNASSIGNED_HOLDINGS
ASPBG
AVWKF
AZFZN
AZVAB
BDRZF
BRXPI
BSCLL
CS3
DCZOG
DPXWK
DR2
EBS
EJD
G-S
GNP
GODZA
HHZ
HZ~
IX1
JPC
KQQ
LAW
LITHE
MY~
OIG
P4E
QRW
R.K
RK2
ROL
RWI
RX1
SUPJJ
W99
WBKPD
WJL
WYJ
XV2
AAYXX
CITATION
ID FETCH-LOGICAL-c1559-9a6d77afd11db60ae4931f7cae1e36d3866119202eae0e122aedf48d84f0501a3
IEDL.DBID DR2
ISSN 0931-7597
IngestDate Thu Oct 10 18:47:42 EDT 2024
Fri Aug 23 01:41:50 EDT 2024
Sat Aug 24 00:55:44 EDT 2024
Wed Oct 30 09:49:55 EDT 2024
IsPeerReviewed false
IsScholarly false
Issue 23
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c1559-9a6d77afd11db60ae4931f7cae1e36d3866119202eae0e122aedf48d84f0501a3
Notes istex:6C05C34DC5FD2422B533896958E0DDDAC905B1DA
ArticleID:CHIN201323039
ark:/67375/WNG-D35BGXLM-7
PQID 1351603241
PQPubID 986341
PageCount 1
ParticipantIDs proquest_journals_1351603241
crossref_primary_10_1002_chin_201323039
wiley_primary_10_1002_chin_201323039_CHIN201323039
istex_primary_ark_67375_WNG_D35BGXLM_7
PublicationCentury 2000
PublicationDate 2013-06-04
June 4, 2013
20130604
PublicationDateYYYYMMDD 2013-06-04
PublicationDate_xml – month: 06
  year: 2013
  text: 2013-06-04
  day: 04
PublicationDecade 2010
PublicationPlace Weinheim
PublicationPlace_xml – name: Weinheim
– name: Frankfurt
PublicationTitle ChemInform
PublicationTitleAlternate ChemInform
PublicationYear 2013
Publisher WILEY-VCH Verlag
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
Publisher_xml – name: WILEY-VCH Verlag
– name: WILEY‐VCH Verlag
– name: Wiley Subscription Services, Inc
References Sonali Kumar, Rashi Sharma, Megan Garcia, Joseph Kamel, Caroline McCarthy, Aaron Muth, Otto IV Phanstiel, Chemoselective Amide Formation Using O-(4-Nitrophenyl)hydroxylamines and Pyruvic Acid Derivatives., J. Org. Chem., 2012, 77, 10835-10845. DOI: 10.1021/jo302175g
2012; 77
e_1_2_2_1_2
References_xml – volume: 77
  start-page: 10835
  year: 2012
  end-page: 10845
  article-title: Chemoselective Amide Formation Using O‐(4‐Nitrophenyl)hydroxylamines and Pyruvic Acid Derivatives.
  publication-title: J. Org. Chem.
– ident: e_1_2_2_1_2
  doi: 10.1021/jo302175g
SSID ssj0023782
Score 1.5449787
Snippet The reaction allows an efficient access to amides.
Abstract The reaction allows an efficient access to amides.
The reaction allows an efficient access to amides. [PUBLICATION ABSTRACT]
SourceID proquest
crossref
wiley
istex
SourceType Aggregation Database
Publisher
StartPage no
SubjectTerms carboxylic amides (acyclic compounds)
Title ChemInform Abstract: Chemoselective Amide Formation Using O-(4-Nitrophenyl)hydroxylamines and Pyruvic Acid Derivatives
URI https://api.istex.fr/ark:/67375/WNG-D35BGXLM-7/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fchin.201323039
https://www.proquest.com/docview/1351603241
Volume 44
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lj9MwELbQcoALb0RhQT4gHofs-pUXt9LSLYgtCLGiN8uviGohi9osonviJ_Ab-SXMOE3YckGCS5RYsRLPeOzP9sw3hDyUnhUmKzgscqxPVMFCUhowd5enRuUACUQMjz6cZdMj9Wqezs9F8bf8EP2GG1pGHK_RwI1d7f8mDUVXQ3TNkgCiJUbwcZmjT9f4Xc8fJaAkHiOUkic5QOeOtZGJ_e3qW7PSRRTwty3IeR64xplncpWY7p9bh5PjvdPG7rmzP-gc_6dR18iVDSylw7YfXScXQn2DXBp12eBukjO8b2OX6NDi_ohrnlEsPFnFVDowatLh54UPdNLFQ9Loj0Df_Pz-44mCy2zRLJHGoF5_evpx7bE90B_R756a2tO36yWG_NChW3g6Bsv4GknJV7fI0eTF-9E02eRtSBwecoKyM5_npvKce5sxExTIv8qdCTzIzMsCMAEASyaCCSxwIUzwlSp8oSqWMm7kbbJTn9ThDqFlsAWvGPSm0qnCWQPrrSqVxhklM1faAXnc6U1_aek5dEvELDTKUveyHJBHUa39a2Z5jE5teao_zA70WKbPD-avD3U-ILud3vXGnlca8xhmDMAnHxARFfiXz-nR9OWsf7r7L5Xukcuizb2RMLVLdprlabgPCKixD2Iv_wV6qf-W
link.rule.ids 315,783,787,1378,27937,27938,46307,46731
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwELagPZQLb9QtBXxAPA5pndh5cVt22W5hNyDUit4svyJWLSnaTRHbEz-B38gvYcbZBJYLElyiJIqV2DNjf-PMfEPIY25ZppIsBCdH20BkzAW5AnM3aaxECpAg8unR0yIZH4vXJ3EbTYi5MA0_RLfhhpbh52s0cNyQ3v_FGoqxhhibxQFF8_wq2QSb52ibw_cdg1TEU18vCvz2MEgBPLe8jSzaX2-_ti5t4hB_XQOdv0NXv_aMbhDdfnUTcnK6d1HrPXP5B6Hjf3XrJrm-Qqa036jSLXLFVbfJ1qAtCHeHXOJ5k75E-xq3SEz9guLN84WvpgMTJ-1_mllHR21KJPUhCfTtj2_fnwk4FLN6jkwG1fLs-celxQ6BSmLoPVWVpe-Wc8z6oX0zs3QIxvHF85Iv7pLj0aujwThYlW4IDP7nBHknNk1VacPQ6oQpJ0AAZWqUCx1PLM8AFgC2ZJFTjrkwipSzpchsJkoWs1Dxe2SjOq_cNqG501lYMlCo3IjMaAUuVxlzZZTgicl1jzxtBSc_NwwdsuFijiSOpezGskeeeLl2j6n5Kca1pbH8UBzIIY9fHpxMpjLtkd1W8HJl0guJpQwTBvgz7JHIS_Avr5OD8WHRXe38S6NHZGt8NJ3IyWHx5j65FjWlOAImdslGPb9wDwAQ1fqhV_mfZfUDvg
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3LbtQwFLWglYANb8RAAS8Qj0VavxIn7IYZplNoQ4WoOjvLsR0xaptWMyliuuIT-Ea-hGtnEjpskGATJVGsxPdhHzv3novQc25JqpOUwiKnsJFIiYsyDe5uZKyFBEjAQnr0Xp6MD8T7STy5lMXf8EN0G27eM8J47R38zJZbv0lDfaihD83iAKJ5dhWtiwTs1cOiTx2BFOMylIuCZTuNJGDnlraRsK3V9ivT0rqX8LcVzHkZuYapZ3QL6fajm4iTo83zutg0F3_wOf5Pr26jm0tcivuNId1BV1x1F10ftOXg7qELf94kL-F-4TdITP0G-5un81BLB4ZN3D-ZWodHbUIkDgEJ-OPP7z9eCTjk03rmeQyqxfHrLwvr-wMG6QPvsa4s3l_MfM4P7pupxUNwja-BlXx-Hx2M3n0ejKNl4YbI-L-coO3ESqlLS6ktEqKdAPmX0mhHHU8sTwEUALIkzGlHHGVMO1uK1KaiJDGhmj9Aa9Vp5R4inLkipSUBc8qMSE2hYcFVxlwbLXhisqKHXrZ6U2cNP4dqmJiZ8rJUnSx76EVQa_eYnh35qDYZq8N8Ww15_HZ7srunZA9ttHpXS4eeK1_IMCGAPmkPsaDAv7xODcY7eXf16F8aPUPX9ocjtbuTf3iMbrCmDkdExAZaq2fn7gmgobp4Ggz-F1ugAm0
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=ChemInform+Abstract%3A+Chemoselective+Amide+Formation+Using+O-%284-Nitrophenyl%29hydroxylamines+and+Pyruvic+Acid+Derivatives&rft.jtitle=ChemInform&rft.au=Kumar%2C+Sonali&rft.au=Sharma%2C+Rashi&rft.au=Garcia%2C+Megan&rft.au=Kamel%2C+Joseph&rft.date=2013-06-04&rft.pub=Wiley+Subscription+Services%2C+Inc&rft.issn=0931-7597&rft.eissn=1522-2667&rft.volume=44&rft.issue=23&rft.spage=no&rft_id=info:doi/10.1002%2Fchin.201323039&rft.externalDBID=NO_FULL_TEXT&rft.externalDocID=2971228161
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0931-7597&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0931-7597&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0931-7597&client=summon