Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Aubert Ribaucourt"'
Autor:
Laia Josa-Culleré, Antti S. K. Lahdenperä, Aubert Ribaucourt, Georg T. Höfler, Serena Gargiulo, Yuan-Yang Liu, Jian-He Xu, Jennifer Cassidy, Francesca Paradisi, Diederik J. Opperman, Frank Hollmann, Caroline E. Paul
Publikováno v:
Catalysts, Vol 9, Iss 3, p 207 (2019)
Redox reactions catalyzed by highly selective nicotinamide-dependent oxidoreductases are rising to prominence in industry. The cost of nicotinamide adenine dinucleotide coenzymes has led to the use of well-established elaborate regeneration systems a
Externí odkaz:
https://doaj.org/article/fee6e17a363448da8c8157a9a007f3e1
Autor:
Janine Cossy, Aubert Ribaucourt
Publikováno v:
ACS Catalysis
ACS Catalysis, American Chemical Society, 2020, 10 (17), pp.10127-10148. ⟨10.1021/acscatal.0c02805⟩
ACS Catalysis, American Chemical Society, 2020, 10 (17), pp.10127-10148. ⟨10.1021/acscatal.0c02805⟩
Transition-metal-catalyzed C(sp2)–N bond forming reactions represent a very active field of research in chemistry. This review outlines the recent developments of the first-row transition-metal-cat...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6e25829e7c164428e390acd0346e101
https://hal.archives-ouvertes.fr/hal-03197958
https://hal.archives-ouvertes.fr/hal-03197958
Publikováno v:
J Am Chem Soc
Herein, we describe a stereodivergent route to (±)-batzelladine D (2), (+)-batzelladine D (2), (−)-batzelladine D (2), and a series of stereochemical analogues and explore their antimicrobial activity for the first time. The concise synthetic appr
A concise synthesis of the tricyclic guanidinium alkaloid batzelladine D has been accomplished in a sequence of 8 steps from readily available building blocks. Highlights of the synthesis include gram-scale preparation of a late stage intermediate, p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b42a14695c484bc807742179cda32aee
https://doi.org/10.26434/chemrxiv.9924692
https://doi.org/10.26434/chemrxiv.9924692
Autor:
Aubert, Ribaucourt, Christopher, Towers, Laia, Josa-Culleré, Frances, Willenbrock, Amber L, Thompson, David M, Hodgson
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
A ring‐closing alkene metathesis (RCM)/ oxyselenation‐selenoxide elimination sequence was established to the sodium salts E‐ and Z‐25 of the originally proposed structure for the recently isolated cytotoxin aruncin B (1), as well as to the so
Autor:
David M. Hodgson, Aubert Ribaucourt
The sodium salts E-15 and Z-15 of the originally proposed dihydropyran acid structure of aruncin B (1) were prepared through ring-closing alkene metathesis (RCM) and ethoxyselenation–selenoxide elimination, but acid sensitivity of these salts, toge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::638473f4a3e450d463158d2f6db84a41
https://doi.org/10.1021/acs.orglett.6b02120
https://doi.org/10.1021/acs.orglett.6b02120
Autor:
Aubert Ribaucourt, Peter W. Smith, David M. Hodgson, Reece Jacques, Ritashree Pal, Nicholas A. Parker, Claire E. Sear
Publikováno v:
ChemInform. 47
In the past two decades, alkene metathesis has risen in prominence to become a significant synthetic strategy for alkene formation. Many total syntheses of natural products have used this transformation. We review the use, from 2003 to 2015, of ring-
Autor:
Peter W. Smith, David M. Hodgson, Reece Jacques, Claire E. Sear, Aubert Ribaucourt, Nicholas A. Parker, Ritashree Pal
Publikováno v:
Organic and Biomolecular Chemistry. 14(25)
In the last two decades, alkene metathesis has risen in prominence to become a significant synthetic strategy for alkene formation. Many total syntheses of natural products have used this transformation. We review the use, from 2003 to 2015, of ring-