Results 231 to 240 of about 18,411 (287)

The continuing significance of chiral agrochemicals

Pest Management Science, Volume 81, Issue 4, Page 1697-1716, April 2025.
In the time frame 2018–2023, around 43% of the 35 chiral agrochemicals introduced to the market (herbicides, fungicides, insecticides, acaricides, and nematicides) contain one or more stereogenic centers in the molecule, and almost 69% of them have been marketed as racemic mixtures of enantiomers or stereoisomers.
Peter Jeschke
wiley   +1 more source

Advances in Vicinal Dicarbo-C-H-functionalization of Five-Membered Heteroarenes via Palladium/Norbornene Cooperative Catalysis. [PDF]

Tetrahedron Lett
Zhou Y, Li R, Ye R, Zhu Q, Liu X, Dong G.   +5 more
europepmc   +1 more source

The Formylation of <i>N</i>,<i>N</i>‑Dimethylcorroles. [PDF]

ACS Omega
Nardis S, Fata A, Pizzoli F, Imbesi G, Petrella G, Cicero DO, Fronczek FR, Smith KM, Paolesse R.   +8 more
europepmc   +1 more source

Comparative Evaluation of Oven, Microwave, and Air-Fry Roasting on Physical Attributes, Bioactive Components, and Volatile Compounds of Rosemary- and Thyme-Coated Mung Bean <i>(</i> <i>Vigna radiata</i> <i>L.)</i>. [PDF]

ACS Omega
Ergun AR, Altay K, Çetintaş Y, Tekgül Barut Y.   +3 more
europepmc   +1 more source

Total Synthesis of Calyciphylline F. [PDF]

Angew Chem Int Ed Engl
Sato R, Sumida R, Inoue M, Kotaka R, Karanjit S, Namba K.   +5 more
europepmc   +1 more source

A Regioselective Approach to Accessing Trisubstituted Pyrrolo[2,3-d][1,2,3]triazoles via an Orthogonal Protection Strategy. [PDF]

Molecules
Brugemann K, Garnier S, Vercouillie J, Routier S, Buron F.   +4 more
europepmc   +1 more source

Synthesis of Stable Betaines Based on 1<i>H</i>-Pyrrole-2,3-diones and Pyridinium Ylides and Their Thermal Conversion to Cyclopropane-Fused Pyrroles. [PDF]

Molecules
Muranova MM, Galeev AR, Mokrushin IG, Maslivets AN, Dmitriev MV.   +4 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Pyrrole Protection

ChemInform, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Benoit Jolicoeur, Erin E. Chapman, Alison Thompson, William D. Lubell   +3 more
openaire   +1 more source

The Oxidation of Pyrrole

Chemistry – An Asian Journal, 2015
AbstractThe dearomatization of heterocycles has been a powerful means for producing functional molecules in synthesis. In the case of pyrroles, reductive methods (such as the Birch reduction) have been most widely exploited, while oxidative methods are generally dismissed as too difficult or unpredictable to be useful.
James K, Howard, Kieran J, Rihak, Alex C, Bissember, Jason A, Smith   +3 more
openaire   +2 more sources

A novel pyrrole synthesis

Org. Biomol. Chem., 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
Sameer, Agarwal, Hans-Joachim, Knolker
openaire   +2 more sources