Organocatalysis stereoselective reactions and applications in organic synthesis

Organocatalysis is considered today one of the three pillars in asymmetric catalysis, along with biocatalysis and organometallic catalysis. The possibility to combine organocatalysis with radical chemistry, photocatalysis and enabling technologies opened new avenues in organic synthesis

Gespeichert in:
Bibliographische Detailangaben
Weitere Verfasser: Benaglia, Maurizio (HerausgeberIn)
Format: Elektronisch E-Book
Sprache:English
Veröffentlicht: Berlin ; Boston De Gruyter [2021]
Schlagworte:
Online-Zugang:FAB01
FAW01
FCO01
FHA01
FKE01
FLA01
UPA01
URL des Erstveröffentlichers
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

MARC

LEADER 00000nmm a2200000 c 4500
001 BV047416355
003 DE-604
005 20220617
007 cr|uuu---uuuuu
008 210812s2021 |||| o||u| ||||||eng d
020 |a 9783110590050  |c PDF  |9 978-3-11-059005-0 
020 |a 9783110588729  |c EPUB  |9 978-3-11-058872-9 
024 7 |a 10.1515/9783110590050  |2 doi 
035 |a (ZDB-23-DGG)9783110590050 
035 |a (OCoLC)1264258719 
035 |a (DE-599)BVBBV047416355 
040 |a DE-604  |b ger  |e rda 
041 0 |a eng 
049 |a DE-1043  |a DE-1046  |a DE-858  |a DE-Aug4  |a DE-859  |a DE-860  |a DE-739  |a DE-83  |a DE-11 
082 0 |a 541.395  |2 23 
084 |a VK 5500  |0 (DE-625)147401:253  |2 rvk 
084 |a VK 5580  |0 (DE-625)147406:253  |2 rvk 
245 1 0 |a Organocatalysis  |b stereoselective reactions and applications in organic synthesis  |c edited by Maurizio Benaglia 
264 1 |a Berlin ; Boston  |b De Gruyter  |c [2021] 
264 4 |c © 2021 
300 |a 1 Online-Ressource (XII, 439 Seiten)  |b Illustrationen 
336 |b txt  |2 rdacontent 
337 |b c  |2 rdamedia 
338 |b cr  |2 rdacarrier 
520 |a Organocatalysis is considered today one of the three pillars in asymmetric catalysis, along with biocatalysis and organometallic catalysis. The possibility to combine organocatalysis with radical chemistry, photocatalysis and enabling technologies opened new avenues in organic synthesis 
650 4 |a Asymmetrische Synthese 
650 4 |a Katalyse 
650 4 |a Organische Syntese 
650 4 |a Organokatalyse 
650 7 |a SCIENCE / Chemistry / Organic  |2 bisacsh 
650 4 |a Catalysis 
650 4 |a Chemistry, Organic 
650 4 |a Stereochemistry 
650 0 7 |a Organokatalyse  |0 (DE-588)7636906-7  |2 gnd  |9 rswk-swf 
650 0 7 |a Stereoselektive Reaktion  |0 (DE-588)4132164-9  |2 gnd  |9 rswk-swf 
689 0 0 |a Organokatalyse  |0 (DE-588)7636906-7  |D s 
689 0 1 |a Stereoselektive Reaktion  |0 (DE-588)4132164-9  |D s 
689 0 |5 DE-604 
700 1 |a Benaglia, Maurizio  |0 (DE-588)1205414207  |4 edt 
776 0 8 |i Erscheint auch als  |n Druck-Ausgabe  |z 978-3-11-058803-3 
856 4 0 |u https://doi.org/10.1515/9783110590050  |x Verlag  |z URL des Erstveröffentlichers  |3 Volltext 
912 |a ZDB-23-DGG 
999 |a oai:aleph.bib-bvb.de:BVB01-032817234 
966 e |u https://doi.org/10.1515/9783110590050  |l FAB01  |p ZDB-23-DGG  |q FAB_PDA_DGG  |x Verlag  |3 Volltext 
966 e |u https://doi.org/10.1515/9783110590050  |l FAW01  |p ZDB-23-DGG  |q FAW_PDA_DGG  |x Verlag  |3 Volltext 
966 e |u https://doi.org/10.1515/9783110590050  |l FCO01  |p ZDB-23-DGG  |q FCO_PDA_DGG  |x Verlag  |3 Volltext 
966 e |u https://doi.org/10.1515/9783110590050  |l FHA01  |p ZDB-23-DGG  |q FHA_PDA_DGG  |x Verlag  |3 Volltext 
966 e |u https://doi.org/10.1515/9783110590050  |l FKE01  |p ZDB-23-DGG  |q FKE_PDA_DGG  |x Verlag  |3 Volltext 
966 e |u https://doi.org/10.1515/9783110590050  |l FLA01  |p ZDB-23-DGG  |q FLA_PDA_DGG  |x Verlag  |3 Volltext 
966 e |u https://doi.org/10.1515/9783110590050  |l UPA01  |p ZDB-23-DGG  |q UPA_PDA_DGG  |x Verlag  |3 Volltext 

Datensatz im Suchindex

_version_ 1804182690630467584
adam_txt
any_adam_object
any_adam_object_boolean
author2 Benaglia, Maurizio
author2_role edt
author2_variant m b mb
author_GND (DE-588)1205414207
author_facet Benaglia, Maurizio
building Verbundindex
bvnumber BV047416355
classification_rvk VK 5500
VK 5580
collection ZDB-23-DGG
ctrlnum (ZDB-23-DGG)9783110590050
(OCoLC)1264258719
(DE-599)BVBBV047416355
dewey-full 541.395
dewey-hundreds 500 - Natural sciences and mathematics
dewey-ones 541 - Physical chemistry
dewey-raw 541.395
dewey-search 541.395
dewey-sort 3541.395
dewey-tens 540 - Chemistry and allied sciences
discipline Chemie / Pharmazie
discipline_str_mv Chemie / Pharmazie
doi_str_mv 10.1515/9783110590050
format Electronic
eBook
fullrecord <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02975nmm a2200625 c 4500</leader><controlfield tag="001">BV047416355</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">20220617 </controlfield><controlfield tag="007">cr|uuu---uuuuu</controlfield><controlfield tag="008">210812s2021 |||| o||u| ||||||eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9783110590050</subfield><subfield code="c">PDF</subfield><subfield code="9">978-3-11-059005-0</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9783110588729</subfield><subfield code="c">EPUB</subfield><subfield code="9">978-3-11-058872-9</subfield></datafield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1515/9783110590050</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ZDB-23-DGG)9783110590050</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)1264258719</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV047416355</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-1043</subfield><subfield code="a">DE-1046</subfield><subfield code="a">DE-858</subfield><subfield code="a">DE-Aug4</subfield><subfield code="a">DE-859</subfield><subfield code="a">DE-860</subfield><subfield code="a">DE-739</subfield><subfield code="a">DE-83</subfield><subfield code="a">DE-11</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">541.395</subfield><subfield code="2">23</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">VK 5500</subfield><subfield code="0">(DE-625)147401:253</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">VK 5580</subfield><subfield code="0">(DE-625)147406:253</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Organocatalysis</subfield><subfield code="b">stereoselective reactions and applications in organic synthesis</subfield><subfield code="c">edited by Maurizio Benaglia</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Berlin ; Boston</subfield><subfield code="b">De Gruyter</subfield><subfield code="c">[2021]</subfield></datafield><datafield tag="264" ind1=" " ind2="4"><subfield code="c">© 2021</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 Online-Ressource (XII, 439 Seiten)</subfield><subfield code="b">Illustrationen</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Organocatalysis is considered today one of the three pillars in asymmetric catalysis, along with biocatalysis and organometallic catalysis. The possibility to combine organocatalysis with radical chemistry, photocatalysis and enabling technologies opened new avenues in organic synthesis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Asymmetrische Synthese</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Katalyse</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Organische Syntese</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Organokatalyse</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SCIENCE / Chemistry / Organic</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Catalysis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chemistry, Organic</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Stereochemistry</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Organokatalyse</subfield><subfield code="0">(DE-588)7636906-7</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Stereoselektive Reaktion</subfield><subfield code="0">(DE-588)4132164-9</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Organokatalyse</subfield><subfield code="0">(DE-588)7636906-7</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Stereoselektive Reaktion</subfield><subfield code="0">(DE-588)4132164-9</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Benaglia, Maurizio</subfield><subfield code="0">(DE-588)1205414207</subfield><subfield code="4">edt</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Erscheint auch als</subfield><subfield code="n">Druck-Ausgabe</subfield><subfield code="z">978-3-11-058803-3</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1515/9783110590050</subfield><subfield code="x">Verlag</subfield><subfield code="z">URL des Erstveröffentlichers</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-23-DGG</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-032817234</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1515/9783110590050</subfield><subfield code="l">FAB01</subfield><subfield code="p">ZDB-23-DGG</subfield><subfield code="q">FAB_PDA_DGG</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1515/9783110590050</subfield><subfield code="l">FAW01</subfield><subfield code="p">ZDB-23-DGG</subfield><subfield code="q">FAW_PDA_DGG</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1515/9783110590050</subfield><subfield code="l">FCO01</subfield><subfield code="p">ZDB-23-DGG</subfield><subfield code="q">FCO_PDA_DGG</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1515/9783110590050</subfield><subfield code="l">FHA01</subfield><subfield code="p">ZDB-23-DGG</subfield><subfield code="q">FHA_PDA_DGG</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1515/9783110590050</subfield><subfield code="l">FKE01</subfield><subfield code="p">ZDB-23-DGG</subfield><subfield code="q">FKE_PDA_DGG</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1515/9783110590050</subfield><subfield code="l">FLA01</subfield><subfield code="p">ZDB-23-DGG</subfield><subfield code="q">FLA_PDA_DGG</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1515/9783110590050</subfield><subfield code="l">UPA01</subfield><subfield code="p">ZDB-23-DGG</subfield><subfield code="q">UPA_PDA_DGG</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield></record></collection>
id DE-604.BV047416355
illustrated Not Illustrated
index_date 2024-07-03T17:55:41Z
indexdate 2024-07-10T09:11:34Z
institution BVB
isbn 9783110590050
9783110588729
language English
oai_aleph_id oai:aleph.bib-bvb.de:BVB01-032817234
oclc_num 1264258719
open_access_boolean
owner DE-1043
DE-1046
DE-858
DE-Aug4
DE-859
DE-860
DE-739
DE-83
DE-11
owner_facet DE-1043
DE-1046
DE-858
DE-Aug4
DE-859
DE-860
DE-739
DE-83
DE-11
physical 1 Online-Ressource (XII, 439 Seiten) Illustrationen
psigel ZDB-23-DGG
ZDB-23-DGG FAB_PDA_DGG
ZDB-23-DGG FAW_PDA_DGG
ZDB-23-DGG FCO_PDA_DGG
ZDB-23-DGG FHA_PDA_DGG
ZDB-23-DGG FKE_PDA_DGG
ZDB-23-DGG FLA_PDA_DGG
ZDB-23-DGG UPA_PDA_DGG
publishDate 2021
publishDateSearch 2021
publishDateSort 2021
publisher De Gruyter
record_format marc
spelling Organocatalysis stereoselective reactions and applications in organic synthesis edited by Maurizio Benaglia
Berlin ; Boston De Gruyter [2021]
© 2021
1 Online-Ressource (XII, 439 Seiten) Illustrationen
txt rdacontent
c rdamedia
cr rdacarrier
Organocatalysis is considered today one of the three pillars in asymmetric catalysis, along with biocatalysis and organometallic catalysis. The possibility to combine organocatalysis with radical chemistry, photocatalysis and enabling technologies opened new avenues in organic synthesis
Asymmetrische Synthese
Katalyse
Organische Syntese
Organokatalyse
SCIENCE / Chemistry / Organic bisacsh
Catalysis
Chemistry, Organic
Stereochemistry
Organokatalyse (DE-588)7636906-7 gnd rswk-swf
Stereoselektive Reaktion (DE-588)4132164-9 gnd rswk-swf
Organokatalyse (DE-588)7636906-7 s
Stereoselektive Reaktion (DE-588)4132164-9 s
DE-604
Benaglia, Maurizio (DE-588)1205414207 edt
Erscheint auch als Druck-Ausgabe 978-3-11-058803-3
https://doi.org/10.1515/9783110590050 Verlag URL des Erstveröffentlichers Volltext
spellingShingle Organocatalysis stereoselective reactions and applications in organic synthesis
Asymmetrische Synthese
Katalyse
Organische Syntese
Organokatalyse
SCIENCE / Chemistry / Organic bisacsh
Catalysis
Chemistry, Organic
Stereochemistry
Organokatalyse (DE-588)7636906-7 gnd
Stereoselektive Reaktion (DE-588)4132164-9 gnd
subject_GND (DE-588)7636906-7
(DE-588)4132164-9
title Organocatalysis stereoselective reactions and applications in organic synthesis
title_auth Organocatalysis stereoselective reactions and applications in organic synthesis
title_exact_search Organocatalysis stereoselective reactions and applications in organic synthesis
title_exact_search_txtP Organocatalysis stereoselective reactions and applications in organic synthesis
title_full Organocatalysis stereoselective reactions and applications in organic synthesis edited by Maurizio Benaglia
title_fullStr Organocatalysis stereoselective reactions and applications in organic synthesis edited by Maurizio Benaglia
title_full_unstemmed Organocatalysis stereoselective reactions and applications in organic synthesis edited by Maurizio Benaglia
title_short Organocatalysis
title_sort organocatalysis stereoselective reactions and applications in organic synthesis
title_sub stereoselective reactions and applications in organic synthesis
topic Asymmetrische Synthese
Katalyse
Organische Syntese
Organokatalyse
SCIENCE / Chemistry / Organic bisacsh
Catalysis
Chemistry, Organic
Stereochemistry
Organokatalyse (DE-588)7636906-7 gnd
Stereoselektive Reaktion (DE-588)4132164-9 gnd
topic_facet Asymmetrische Synthese
Katalyse
Organische Syntese
Organokatalyse
SCIENCE / Chemistry / Organic
Catalysis
Chemistry, Organic
Stereochemistry
Stereoselektive Reaktion
url https://doi.org/10.1515/9783110590050
work_keys_str_mv AT benagliamaurizio organocatalysisstereoselectivereactionsandapplicationsinorganicsynthesis