author_facet Radcliffe, James E.
Fasano, Valerio
Adams, Ralph W.
You, Peiran
Ingleson, Michael J.
Radcliffe, James E.
Fasano, Valerio
Adams, Ralph W.
You, Peiran
Ingleson, Michael J.
author Radcliffe, James E.
Fasano, Valerio
Adams, Ralph W.
You, Peiran
Ingleson, Michael J.
spellingShingle Radcliffe, James E.
Fasano, Valerio
Adams, Ralph W.
You, Peiran
Ingleson, Michael J.
Chemical Science
Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
General Chemistry
author_sort radcliffe, james e.
spelling Radcliffe, James E. Fasano, Valerio Adams, Ralph W. You, Peiran Ingleson, Michael J. 2041-6520 2041-6539 Royal Society of Chemistry (RSC) General Chemistry http://dx.doi.org/10.1039/c8sc04305a <p>The combination of NHC–BH<sub>3</sub>/I<sub>2</sub> represents a simple method for the reductive α-borylation of α,β-unsaturated esters to form useful α-boryl esters.</p> Reductive α-borylation of α,β-unsaturated esters using NHC–BH<sub>3</sub> activated by I<sub>2</sub> as a metal-free route to α-boryl esters Chemical Science
doi_str_mv 10.1039/c8sc04305a
facet_avail Online
Free
format ElectronicArticle
fullrecord blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAzOS9jOHNjMDQzMDVh
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAzOS9jOHNjMDQzMDVh
institution DE-Pl11
DE-Rs1
DE-105
DE-14
DE-Ch1
DE-L229
DE-D275
DE-Bn3
DE-Brt1
DE-Zwi2
DE-D161
DE-Gla1
DE-Zi4
DE-15
imprint Royal Society of Chemistry (RSC), 2019
imprint_str_mv Royal Society of Chemistry (RSC), 2019
issn 2041-6520
2041-6539
issn_str_mv 2041-6520
2041-6539
language English
mega_collection Royal Society of Chemistry (RSC) (CrossRef)
match_str radcliffe2019reductiveaborylationofabunsaturatedestersusingnhcbh3activatedbyi2asametalfreeroutetoaborylesters
publishDateSort 2019
publisher Royal Society of Chemistry (RSC)
recordtype ai
record_format ai
series Chemical Science
source_id 49
title Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
title_unstemmed Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
title_full Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
title_fullStr Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
title_full_unstemmed Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
title_short Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
title_sort reductive α-borylation of α,β-unsaturated esters using nhc–bh<sub>3</sub> activated by i<sub>2</sub> as a metal-free route to α-boryl esters
topic General Chemistry
url http://dx.doi.org/10.1039/c8sc04305a
publishDate 2019
physical 1434-1441
description <p>The combination of NHC–BH<sub>3</sub>/I<sub>2</sub> represents a simple method for the reductive α-borylation of α,β-unsaturated esters to form useful α-boryl esters.</p>
container_issue 5
container_start_page 1434
container_title Chemical Science
container_volume 10
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
_version_ 1792338573428523021
geogr_code not assigned
last_indexed 2024-03-01T15:34:23.503Z
geogr_code_person not assigned
openURL url_ver=Z39.88-2004&ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fvufind.svn.sourceforge.net%3Agenerator&rft.title=Reductive+%CE%B1-borylation+of+%CE%B1%2C%CE%B2-unsaturated+esters+using+NHC%E2%80%93BH3+activated+by+I2+as+a+metal-free+route+to+%CE%B1-boryl+esters&rft.date=2019-01-01&genre=article&issn=2041-6539&volume=10&issue=5&spage=1434&epage=1441&pages=1434-1441&jtitle=Chemical+Science&atitle=Reductive+%CE%B1-borylation+of+%CE%B1%2C%CE%B2-unsaturated+esters+using+NHC%E2%80%93BH%3Csub%3E3%3C%2Fsub%3E+activated+by+I%3Csub%3E2%3C%2Fsub%3E+as+a+metal-free+route+to+%CE%B1-boryl+esters&aulast=Ingleson&aufirst=Michael+J.&rft_id=info%3Adoi%2F10.1039%2Fc8sc04305a&rft.language%5B0%5D=eng
SOLR
_version_ 1792338573428523021
author Radcliffe, James E., Fasano, Valerio, Adams, Ralph W., You, Peiran, Ingleson, Michael J.
author_facet Radcliffe, James E., Fasano, Valerio, Adams, Ralph W., You, Peiran, Ingleson, Michael J., Radcliffe, James E., Fasano, Valerio, Adams, Ralph W., You, Peiran, Ingleson, Michael J.
author_sort radcliffe, james e.
container_issue 5
container_start_page 1434
container_title Chemical Science
container_volume 10
description <p>The combination of NHC–BH<sub>3</sub>/I<sub>2</sub> represents a simple method for the reductive α-borylation of α,β-unsaturated esters to form useful α-boryl esters.</p>
doi_str_mv 10.1039/c8sc04305a
facet_avail Online, Free
format ElectronicArticle
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
geogr_code not assigned
geogr_code_person not assigned
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAzOS9jOHNjMDQzMDVh
imprint Royal Society of Chemistry (RSC), 2019
imprint_str_mv Royal Society of Chemistry (RSC), 2019
institution DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-Zwi2, DE-D161, DE-Gla1, DE-Zi4, DE-15
issn 2041-6520, 2041-6539
issn_str_mv 2041-6520, 2041-6539
language English
last_indexed 2024-03-01T15:34:23.503Z
match_str radcliffe2019reductiveaborylationofabunsaturatedestersusingnhcbh3activatedbyi2asametalfreeroutetoaborylesters
mega_collection Royal Society of Chemistry (RSC) (CrossRef)
physical 1434-1441
publishDate 2019
publishDateSort 2019
publisher Royal Society of Chemistry (RSC)
record_format ai
recordtype ai
series Chemical Science
source_id 49
spelling Radcliffe, James E. Fasano, Valerio Adams, Ralph W. You, Peiran Ingleson, Michael J. 2041-6520 2041-6539 Royal Society of Chemistry (RSC) General Chemistry http://dx.doi.org/10.1039/c8sc04305a <p>The combination of NHC–BH<sub>3</sub>/I<sub>2</sub> represents a simple method for the reductive α-borylation of α,β-unsaturated esters to form useful α-boryl esters.</p> Reductive α-borylation of α,β-unsaturated esters using NHC–BH<sub>3</sub> activated by I<sub>2</sub> as a metal-free route to α-boryl esters Chemical Science
spellingShingle Radcliffe, James E., Fasano, Valerio, Adams, Ralph W., You, Peiran, Ingleson, Michael J., Chemical Science, Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters, General Chemistry
title Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
title_full Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
title_fullStr Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
title_full_unstemmed Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
title_short Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
title_sort reductive α-borylation of α,β-unsaturated esters using nhc–bh<sub>3</sub> activated by i<sub>2</sub> as a metal-free route to α-boryl esters
title_unstemmed Reductive α-borylation of α,β-unsaturated esters using NHC–BH3 activated by I2 as a metal-free route to α-boryl esters
topic General Chemistry
url http://dx.doi.org/10.1039/c8sc04305a