Results 151 to 160 of about 18,820,263 (207)

One-pot synthesis of primary phosphines from white phosphorus.

open access: yesChem Commun (Camb)
Mende M, Cammarata J, Scott DJ, Wolf R.
europepmc   +1 more source
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One Pot Synthesis of Methyl Aminoacetylcyanoacetates

Synthetic Communications, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Stylianos Hamilakis, Athanase Tsolomitis
openaire   +1 more source

One-Pot Synthesis of Glucosamine Oligosaccharides

Organic Letters, 2001
[reaction: see text] Tuning the reactivity of glycosyl donors derived from 2-amino-2-deoxy glucose by selective introduction of different N-protecting (NPhth and NHTroc) and anomeric leaving groups (ethylthio and phenylthio) enabled highly efficient oligosaccharide synthesis in a one-pot manner.
Micha, Fridman   +3 more
openaire   +2 more sources

Programmable One-Pot Synthesis of Oligosaccharides

Biochemistry, 2019
Carbohydrates make up one of the four major classes of biomolecules, often conjugated with proteins as glycoproteins or with lipids as glycolipids, and participate in many important biochemical functions in living species. However, glycoproteins or glycolipids often exist as mixtures, and as a consequence, it is difficult to isolate individual ...
Cheng-Wei Cheng   +3 more
openaire   +2 more sources

A New One-Pot Synthesis of Alkynylphosphonates

Organic Letters, 2000
A method for the palladium-catalyzed synthesis of alkynylphosphonates from 1,1-dibromo-1-alkenes has been developed. In general, the best catalyst system for this transformation was found to be Pd(OAc)(2), dppf, H-phosphonate, propylene oxide, DMF, 80 degrees C.
, Lera, , Hayes
openaire   +2 more sources

A Simple One-Pot Synthesis of Methyltribromosilane

Phosphorus, Sulfur, and Silicon and the Related Elements, 2007
A simple one-pot synthesis of methyltribromosilane has been developed. The straightforward reaction of a slight excess of silicon tetrabromide with one equivalent of powdered methyllithium in refluxing pentane produces methyltribromosilane in high yields.
Pitcher, MW, Bianconi, PA
openaire   +1 more source

Stereoselective One-Pot Synthesis of Oxazolines

The Journal of Organic Chemistry, 2008
Treatment of alkenes with NBS, a nitrile, NaHCO3 and water in the presence of Cu(OTf)2 or Zn(OTf)2 is reported to furnish oxazolines in one pot and good yields. The reaction is equally applicable to chalcones.
Saumen, Hajra   +3 more
openaire   +2 more sources

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