Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Primali V. Navaratne"'
Autor:
Ion Ghiviriga, Kavindri D. Ranasinghe, Primali V. Navaratne, Jenny L. Wilkerson, Jasmine S. Felix, Lance R. McMahon, Evgeniya Semenova, Adrian E. Roitberg, Alexander J. Grenning
Publikováno v:
ChemMedChem
Phytocannabinoids (and synthetic analogs thereof) are gaining significant attention as promising leads in modern medicine. Considering this, new directions for the design of phytocannabinoid-inspired molecules is of immediate interest. In this regard
Publikováno v:
Organic & Biomolecular Chemistry. 15:69-75
A simple platform for carbocycle synthesis by Knoevenagel adduct deconjugative alkylation/Heck reaction is described. Deconjugative alkylation of Knoevenagels adducts is two-fold synthetically enabling because C-C bond formation is (1) operationally
Autor:
Adrian E. Roitberg, Lance R. McMahon, Evgeniya Semenova, Jenny L. Wilkerson, Ion Ghivirga, Kavindri D. Ranasinghe, Alex Grenning, Primali V. Navaratne
Phytocannabinoids, molecules isolated from cannabis, are gaining attention as promising leads in modern medicine, including pain management. Considering the urgent need for combating the opioid crisis, new directions for the design of cannabinoid-ins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df4e8269d30a2259a09fca908290d2e6
https://doi.org/10.26434/chemrxiv.10251035.v1
https://doi.org/10.26434/chemrxiv.10251035.v1
Autor:
Primali V. Navaratne, Alexander J. Grenning, Kavindri D. Ranasinghe, Lance R. McMahon, Jenny L. Wilkerson, Evgeniya Semenova, Ion Ghiviriga, Jasmine S. Felix, Adrian E. Roitberg
Publikováno v:
ChemMedChem. 15:727-727
Publikováno v:
Organic letters. 20(15)
A modular and practical route to versatile cyano-1,3-dienes by a sequence involving deconjugative alkylation and "Tsuji-Saegusa-Ito oxidation" is reported. In this letter, the versatility of the products is also explored, including a route to benzoch
Publikováno v:
ChemInform. 47
Knoevenagel adducts derived from readily available acetoxyacetone and malonic acid derivatives served as trimethylenemethane surrogates for formal 1,3-difunctionalization through a sequence of selective γ-deprotonation/α-alkylation and palladium(0)
Publikováno v:
Angewandte Chemie (International ed. in English). 55(1)
Knoevenagel adducts derived from readily available acetoxyacetone and malonic acid derivatives served as trimethylenemethane surrogates for formal 1,3-difunctionalization through a sequence of selective γ-deprotonation/α-alkylation and palladium(0)
Publikováno v:
Angewandte Chemie. 1/4/2016, Vol. 128 Issue 1, p325-328. 4p.
Autor:
Navaratne, Primali V., Wilkerson, Jenny L., Ranasinghe, Kavindri D., Semenova, Evgeniya, Felix, Jasmine S., Ghiviriga, Ion, Roitberg, Adrian, McMahon, Lance R., Grenning, Alexander J.
Publikováno v:
ChemMedChem; 5/6/2020, Vol. 15 Issue 9, p727-727, 1p
Autor:
Navaratne, Primali V., Wilkerson, Jenny L., Ranasinghe, Kavindri D., Semenova, Evgeniya, Felix, Jasmine S., Ghiviriga, Ion, Roitberg, Adrian, McMahon, Lance R., Grenning, Alexander J.
Publikováno v:
ChemMedChem; 5/6/2020, Vol. 15 Issue 9, p728-732, 5p