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About:
Generation and cyclization of unsaturated carbamoyl radicals derived from S-4-pentynyl carbamothioates under tin-free conditions
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rdf:type
Item
description
artículu científicu
(ast)
wetenschappelijk artikel
(nl)
article scientifique publié en 2006
(fr)
наукова стаття, опублікована у квітні 2006
(uk)
im April 2006 veröffentlichter wissenschaftlicher Artikel
(de)
publication date
wds:Q56998353-A42E8807-EE9D-475F-B374-394DDE0D3B23
publication date
2006-04-14 00:00:00Z
(
xsd:dateTime
)
language of work or name
wds:Q56998353-00F9EA41-2CF3-404E-94AA-96EA98D4ACAC
language of work or name
English
author name string
wds:Q56998353-08401A51-1384-47E9-89F1-8F49DF3F8BB9
wds:Q56998353-0C179428-B1AB-4D19-94F2-87940A738598
wds:Q56998353-339D1B3C-2826-4A32-A062-E746593235D8
wds:Q56998353-98794FDC-6624-40A3-8822-09382C78BF9B
wds:Q56998353-A65B95E5-F12B-4E12-B49C-CCF71D831C39
wds:Q56998353-EFF5009D-531C-4859-BDDE-0FB68366A2F3
author name string
Rino Leardini
Matteo Minozzi
Piero Spagnolo
Giuseppe Zanardi
Luisa Benati
Rosanna Scialpi
rdfs:label
Generation and cyclization of unsaturated carbamoyl radicals derived from S-4-pentynyl carbamothioates under tin-free conditions
(en)
Generation and cyclization of unsaturated carbamoyl radicals derived from S-4-pentynyl carbamothioates under tin-free conditions
(nl)
skos:prefLabel
Generation and cyclization of unsaturated carbamoyl radicals derived from S-4-pentynyl carbamothioates under tin-free conditions
(en)
Generation and cyclization of unsaturated carbamoyl radicals derived from S-4-pentynyl carbamothioates under tin-free conditions
(nl)
name
Generation and cyclization of unsaturated carbamoyl radicals derived from S-4-pentynyl carbamothioates under tin-free conditions
(en)
Generation and cyclization of unsaturated carbamoyl radicals derived from S-4-pentynyl carbamothioates under tin-free conditions
(nl)
author
wds:Q56998353-133E92DF-47BB-40AD-90AA-8A66DA67E7CD
wds:Q56998353-C7797A01-3564-4FD4-9DC2-7048F0E8F88C
author
Daniele Nanni
Giorgio Bencivenni
title
wds:Q56998353-7C95C1F6-8DB9-4843-AAE7-BC98B5B651D6
title
Generation and cyclization of unsaturated carbamoyl radicals derived from S-4-pentynyl carbamothioates under tin-free conditions
(en)
page(s)
wds:Q56998353-41A3ED22-227A-4FEB-80A9-C22B48A5F5F6
page(s)
3192-7
instance of
wds:Q56998353-3140AF83-893D-4321-8127-CB448F8A6E86
instance of
scholarly article
PubMed ID
wds:Q56998353-9EE2F826-A985-404D-B773-5686D664BB23
PubMed ID
http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16599618
PubMed ID
16599618
published in
wds:Q56998353-156C528E-8ABF-472A-8B82-FAB0F4F6BA3E
published in
Journal of Organic Chemistry
issue
wds:Q56998353-4F1893D3-F9EF-4760-AA9B-BE28969B510F
volume
wds:Q56998353-CEAD2B09-3FB7-4968-AA28-250AE42CFC32
issue
8
volume
71
DOI
wds:Q56998353-4F7CBA03-8494-4578-9F83-E916588732D6
DOI
http://dx.doi.org/10.1021/JO0602064
DOI
10.1021/JO0602064
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about
of
https://www.wikidata.org/wiki/Special:EntityData/Q56998353
is
cites work
of
New applications of dithiocarbamates in organic synthesis
Carbamoyl radical-mediated synthesis and semipinacol rearrangement of β-lactam diols.
A New Method of Synthesis of 6-Substituted Piperidine-2,4-diones from Homoallylamines
Thiomaleic anhydride: a convenient building block for the synthesis of alpha-substituted gamma- and delta-lactones through free-radical addition, nucleophilic ring opening, and subsequent thiocarboxylate manipulation
Thiols, thioethers, and related compounds as sources of C-centred radicals
Photoredox-catalyzed procedure for carbamoyl radical generation: 3,4-dihydroquinolin-2-one and quinolin-2-one synthesis.
is
cites work
of
wds:Q57351242-C803CF5F-CF6B-4C20-979B-E86B9DB287B7
wds:Q42640859-6E4585A7-6F3E-4394-8774-FEB62F22756B
wds:Q38119415-00879FC2-D7AA-433B-B21E-CE831015E2FC
wds:Q35061109-75E7086D-20A6-4BCE-B1E2-074192F90549
wds:Q57998860-FB705E14-B89E-46CD-B112-9D3230053610
wds:Q48198323-D3BC6879-7E37-4B35-BA0E-414CD43763D7
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