Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Daniel S. Müller"'
Autor:
Daniel S. Müller
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 787-814 (2024)
The hydrochlorination of alkenes has been extensively studied in research and is commonly featured in organic chemistry textbooks as an exemplification of the Markovnikov rule. However, the application of this reaction is typically limited to specifi
Externí odkaz:
https://doaj.org/article/f52902f7062f4dffa150e03683394c6e
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2999-3010 (2018)
Stereoretentive olefin metathesis based on ruthenium dithiolate complexes has become a very active field of research within the past years. This unique catalyst class is able to kinetically produce both Z- and E-alkenes in high stereochemical purity
Externí odkaz:
https://doaj.org/article/19c6b644d8684e72b987ce6d5dbe53db
Autor:
Olivier Baslé, Idriss Curbet, Thierry Roisnel, Alexandre Quelhas, Daniel S. Müller, Marc Mauduit, Romane Manguin, Yann Trolez, Sophie Colombel-Rouen, Anthony Clermont
Publikováno v:
Chemical Science
Chemical Science, 2020, 11 (19), pp.4934-4938. ⟨10.1039/d0sc01124j⟩
Chemical Science, The Royal Society of Chemistry, 2020, 11 (19), pp.4934-4938. ⟨10.1039/d0sc01124j⟩
Chemical Science, 2020, 11 (19), pp.4934-4938. ⟨10.1039/d0sc01124j⟩
Chemical Science, The Royal Society of Chemistry, 2020, 11 (19), pp.4934-4938. ⟨10.1039/d0sc01124j⟩
International audience; The first synthesis of conjugated triynes by molybdenum-catalysed alkyne metathesis is reported. Strategic to the success of this approach is the utilization of sterically-hindered diynes that allowed for the site-selective al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bad417aefb2cfded9816a6a04a43f422
https://hal.science/hal-02886437/file/d0sc01124j.pdf
https://hal.science/hal-02886437/file/d0sc01124j.pdf
Publikováno v:
Angewandte Chemie International Edition. 56:6783-6787
The highly diastereo- and enantioselective formation of polysubstituted cyclopropanes was easily achieved through the asymmetric copper-catalyzed carbomagnesiation reaction of nonfunctionalized cyclopropene derivatives. The carbometalated species gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cf9e90e01528e89089a0b608b8f5338
https://doi.org/10.1002/anie.201701094
https://doi.org/10.1002/anie.201701094
Autor:
Romane Manguin, Anthony Clermont, Yann Trolez, Olivier Baslé, Thierry Roisnel, Idriss Curbet, Marc Mauduit, Alexandre Quelhas, Daniel S. Müller, Sophie Colombel-Rouen
The synthesis of conjugated triynes by molybdenum-catalyzed alkyne metathesis is reported. Strategic to the success of this approach is the utilization of sterically-hindered diynes that allowed for the site- selective alkyne metathesis to produce th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c16a8e2ae7baa953712f68bcee3d8b6
https://doi.org/10.26434/chemrxiv.8342534.v1
https://doi.org/10.26434/chemrxiv.8342534.v1
Publikováno v:
ACS Catalysis
ACS Catalysis, 2019, 9 (4), pp.3511-3518. ⟨10.1021/acscatal.9b00244⟩
ACS Catalysis, American Chemical Society, 2019, 9 (4), pp.3511-3518. ⟨10.1021/acscatal.9b00244⟩
ACS Catalysis, 2019, 9 (4), pp.3511-3518. ⟨10.1021/acscatal.9b00244⟩
ACS Catalysis, American Chemical Society, 2019, 9 (4), pp.3511-3518. ⟨10.1021/acscatal.9b00244⟩
International audience; A systematic study for the in situ generation of Ru-based metathesis catalysts was described. Assembly of commercially available and inexpensive reagents [Ru(p-cymene)Cl-2](2), SIPr center dot HCl, and n-BuLi led to the format
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93e1395161dae5433d1eb24ed1fe46d1
https://univ-rennes.hal.science/hal-02115712
https://univ-rennes.hal.science/hal-02115712
Autor:
Daniel S. Müller, Larry E. Overman, Gregory L. Lackner, Nicholas L. Untiedt, Christopher R. Jamison, André P. Dieskau, Yuriy Slutskyy
Publikováno v:
The Journal of Organic Chemistry
The evolution of a convergent fragment-coupling strategy for the enantioselective total synthesis of trans-clerodane diterpenoids is described. The key bond construction is accomplished by 1,6-addition of a trans-decalin tertiary radical with 4-vinyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72aedf9557d9f52c5c793b0bb60ed45b
https://doi.org/10.1021/acs.joc.6b00697
https://doi.org/10.1021/acs.joc.6b00697
Autor:
Ilan Marek, Daniel S. Müller
Publikováno v:
Chemical Society Reviews. 45:4552-4566
Since the first discovery of carbocupration of alkynes in the 1970s a tremendous amount of research has been carried out in this field. The exceptionally high selectivities obtained attribute to the great synthetic value of carbocupration reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41bb39945d2b9dacc2a2f0db118f02af
https://doi.org/10.1039/c5cs00897b
https://doi.org/10.1039/c5cs00897b
Autor:
Ilan Marek, Daniel S. Müller
Publikováno v:
Journal of the American Chemical Society. 137:15414-15417
The enantioselective synthesis of cyclopropylzinc reagents has been achieved via a copper-catalyzed carbozincation of 3,3-disubstituted cyclopropenes with diorganozinc reagents. The obtained organozinc compounds can be easily functionalized with a br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f019c501f6f724a5640dbf44f552f996
https://doi.org/10.1021/jacs.5b11220
https://doi.org/10.1021/jacs.5b11220
Autor:
Idriss Curbet, Adrien Dumas, Olivier Baslé, Loïc Toupet, Marc Mauduit, Daniel S. Müller, Mathieu Rouen
Publikováno v:
Organometallics
Organometallics, 2018, 37 (5), pp.829-834. ⟨10.1021/acs.organomet.7b00836⟩
Organometallics, American Chemical Society, 2018, 37 (5), pp.829-834. ⟨10.1021/acs.organomet.7b00836⟩
Organometallics, 2018, 37 (5), pp.829-834. ⟨10.1021/acs.organomet.7b00836⟩
Organometallics, American Chemical Society, 2018, 37 (5), pp.829-834. ⟨10.1021/acs.organomet.7b00836⟩
International audience; A series of new stereoretentive ruthenium catalysts bearing the dithiocatecholate ligand was synthesiszed on the basis of the M7 and Ru-benzylidene-oxazinone design. The activity of the catalysts was tested in ring-opening cro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f27882eb005610764f9747b1e99847d9
https://univ-rennes.hal.science/hal-01771077
https://univ-rennes.hal.science/hal-01771077