Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Saumya Dabral"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 1788-1795 (2017)
A lipase-catalyzed esterification of lignin model compounds in the ball mill was developed combining the advantages of enzyme catalysis and mechanochemistry. Under the described conditions, the primary aliphatic hydroxy groups present in the substrat
Externí odkaz:
https://doaj.org/article/38551420e10c46f29e89fed066a845bc
Publikováno v:
Molecules, Vol 22, Iss 1, p 146 (2017)
A mechanochemical Strecker reaction involving a wide range of aldehydes (aromatic, heteroaromatic and aliphatic), amines, and KCN afforded a library of α-aminonitriles upon mechanical activation. This multicomponent process was efficiently activated
Externí odkaz:
https://doaj.org/article/ddf2e4021b4a4004b9fef9fb28d1282c
Autor:
Chloë Johnson, A. Stephen K. Hashmi, Saumya Dabral, Ulrike Licht, Thomas Schaub, Peter Rudolf
Publikováno v:
ChemCatChem. 13:353-361
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b48b9906630db3fd7c636f01a713c7e1
https://doi.org/10.1002/cctc.202001551
https://doi.org/10.1002/cctc.202001551
Autor:
Saumya Dabral, A. Stephen K. Hashmi, Ulrike Licht, Gérard Bollmann, Peter Rudolf, Thomas Schaub
Publikováno v:
Green Chemistry. 22:1553-1558
Using the bulk chemical 1,4-butynediol, readily available epoxides and carbon dioxide, a new series of unsubstituted exovinylene carbonates were synthesised. Chemoselective additions of diamines or diols to these cyclic carbonates allow the regiocont
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45262ad379b5a89a7b8792406ac3282d
https://doi.org/10.1039/c9gc04320a
https://doi.org/10.1039/c9gc04320a
Autor:
Saumya Dabral, Bilguun Bayarmagnai, Thomas Schaub, Jasmin Schießl, Marko Hermsen, A. Stephen K. Hashmi, Verena Mormul
Publikováno v:
Organic Letters. 21:1422-1425
By using silver complexes with bulky ligands such as DavePhos or N-heterocyclic carbenes, propargylic alcohols are smoothly converted with CO2 into a unique class of unexplored cyclic alkylidene carbonates. These systems, for the first time, also ach
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ffb347ff28b90c23b3d0c7d01988ec2
https://doi.org/10.1021/acs.orglett.9b00156
https://doi.org/10.1021/acs.orglett.9b00156
Publikováno v:
ACS Sustainable Chemistry & Engineering. 6:3242-3254
A mechanochemical oxidation and cleavage reaction in lignin β-O-4 model compounds and lignin catalyzed by HO–TEMPO/KBr/Oxone (TEMPO is 2,2,6,6-tetramethyl-1-piperidinyloxy) has been developed under milling conditions. The studies on nonphenolic li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff82a468c10341cfb9e81fbe621ce863
https://doi.org/10.1021/acssuschemeng.7b03418
https://doi.org/10.1021/acssuschemeng.7b03418
Autor:
Ciaran W. Lahive, Carsten Bolm, Stephanie S. M. Spoehrle, Saumya Dabral, Julien Engel, Jakob Mottweiler
Publikováno v:
Green Chemistry. 20:170-182
The depleting fossil reservoirs have stimulated global research initiatives on renewable lignin feedstocks as sustainable alternatives to petroleum-derived aromatics. Base-catalysed depolymerisation (BCD) is regarded as an economical and efficient ap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ddbaade9c2de4d07bd7e48feaf60abd
https://doi.org/10.1039/c7gc03110f
https://doi.org/10.1039/c7gc03110f
Publikováno v:
Organic letters. 19(16)
An atom transfer radical addition elimination (ATRE) reaction of terminal alkenes with perfluoroalkyl halides under visible light is described. The photoredox catalysis with Eosin Y provides perfluoroalkenes in good yields. The reaction has been util
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b7ea4fd365d105cf6d0043f4e5cae8a
https://pubmed.ncbi.nlm.nih.gov/28766948
https://pubmed.ncbi.nlm.nih.gov/28766948
Publikováno v:
ChemSusChem. 10(13)
This research was supported by the European Union (Marie Curie ITN “SuBiCat” PITN-GA-2013-607044, S.D.) and by the Distinguished Professorship Program at RWTH Aachen University funded by the Excellence Initiative of the German federal and state g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f879f2cbd2bf58f50eb87da9bfe45b2a
https://pubmed.ncbi.nlm.nih.gov/28523820
https://pubmed.ncbi.nlm.nih.gov/28523820
Publikováno v:
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules 22(1), 146 (2017). doi:10.3390/molecules22010146
Molecules; Volume 22; Issue 1; Pages: 146
Molecules, Vol 22, Iss 1, p 146 (2017)
Molecules 22(1), 146 (2017). doi:10.3390/molecules22010146
Molecules; Volume 22; Issue 1; Pages: 146
Molecules, Vol 22, Iss 1, p 146 (2017)
A mechanochemical Strecker reaction involving a wide range of aldehydes (aromatic, heteroaromatic and aliphatic), amines, and KCN afforded a library of α-aminonitriles upon mechanical activation. This multicomponent process was efficiently activated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c756700aef4ef540c877ccdd8f5a97bb
https://pubmed.ncbi.nlm.nih.gov/28106742
https://pubmed.ncbi.nlm.nih.gov/28106742