Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ritashree Pal"'
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
We show that readily available α‐amidoaldehydes are effective substrates for intermolecular Rh‐catalyzed alkyne hydroacylation reactions. The catalyst [Rh(dppe)(C6H5F)][BArF 4] provides good reactivity, and allows a broad range of aldehydes and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c0799dc1a094239dcf7eef76fb1f687
https://doi.org/10.1002/chem.202002478
https://doi.org/10.1002/chem.202002478
Publikováno v:
Tetrahedron Letters. 56:6210-6213
N-Boc/MOM-protected furoindolones, synthesized in four steps, have been successfully employed in the Hauser annulations with Michael acceptors to provide a new synthesis of carbazole-1,4-quinones. This methodology works well with a number of acceptor
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-
Publikováno v:
ChemInform. 47
A facile protocol for annulation reactions of furoindolones with Michael acceptors or aryne precursors is presented.