Results 201 to 210 of about 51,028 (331)

Synthesis of acyl(chloro)phosphines enabled by phosphinidene transfer

, 2019
Kevin M. Szkop, Michael B. Geeson, Douglas W. Stephan, Christopher C. Cummins   +3 more
openalex   +2 more sources

Fluorogenic Coumarins Activated via Bioorthogonal Reactions. [PDF]

J Org Chem
Lin-Jones HM, Chen S, Seo Y, Pham KQ, Prescher JA.   +4 more
europepmc   +1 more source

The versatile synthesis and biological evaluation of all-alkyl biscationic quaternary phosphonium compounds: atom-economical and potent disinfectants. [PDF]

RSC Med Chem
McDonough D, Bezold EL, Wuest WM, Minbiole KPC.   +3 more
europepmc   +1 more source

Stabilisation of Red Phosphorus to Prevent Moisture Absorption and Suppression of Phosphine Release

, 2007
M. R. Somayajulu, Garima Gautam, A. Subhananda Rao   +2 more
openalex   +1 more source

Phosphazenyl Phosphine Proton Sponges: Does the Proton-Chelating Effect Enhance Their Basicity? [PDF]

Int J Mol Sci
Glasovac Z, Barić D, Despotović I, Kovačević B.   +3 more
europepmc   +1 more source

Optical Properties of Heavily Fluorinated Lanthanide Tris β-Diketonate Phosphine Oxide Adducts [PDF]

, 2016
Adam N. Swinburne, Madeleine Langford Paden, Tsz Chan, Simon Randall, Fabrizio Ortu, Alan M. Kenwright, Louise S. Natrajan   +6 more
openalex   +1 more source

Direct Editing of Cysteine to Electrophilic Alkyl Halides in Peptides. [PDF]

J Am Chem Soc
Honeycutt DS, Salgado-Bello W, Greenberg HS, McCarthy WK, Mrosla JM, Pallares B, Goldberg JM, Wang F.   +7 more
europepmc   +1 more source

Synthesis, Study, and Catalysis of New Dimethyl-Phosphine Ligands

, 2016
Alexander J. Kendall
openalex   +1 more source

Preparation and Reactivity of Acyclic (Pentadienyl)iron(1+) Cations: Applications to Organic Synthesis [PDF]

, 1997
Donaldson, William A.
core   +1 more source

Intermolecular Enantioselective Nickel‐Catalyzed Arylation of Un‐Activated C(sp3)─H Bond

Angewandte Chemie International Edition, EarlyView.
Ni: a new solution for asymmetric C(sp3)─H activation. The stereoselective synthesis of all‐carbon quaternary stereogenic centres is achieved via enantioselective C(sp3)─H arylation using a Ni‐BINOL‐derived catalyst. Rational catalytic cycle design uncovers a new reaction pathway that can efficiently induce chiral information during the stereoselective
Erwan Brunard, Fengjie Huang, Àlex Díaz‐Jiménez, Sofiya Kostiukovska, Joanna Wencel‐Delord   +4 more
wiley   +1 more source