Results 161 to 170 of about 2,093,167 (240)

An on-surface Diels-Alder reaction. [PDF]

Angew Chem Int Ed Engl, 2021
Castro-Esteban J, Albrecht F, Fatayer S, Pérez D, Gross L, Peña D.   +5 more
europepmc   +1 more source

Inverse-Electron-Demand Diels-Alder Reaction of Tropone with Graphene Supported on Cu(111). [PDF]

Small
Tu J, Zhou W, Wolf LM, Yan M.
europepmc   +1 more source

Fibrillar Hydrogel Based on Cellulose Nanocrystals Crosslinked via Diels-Alder Reaction: Preparation and pH-Sensitive Release of Benzocaine. [PDF]

Polymers (Basel), 2023
Morozova SM, Korzhikova-Vlakh EG.
europepmc   +1 more source

Recent Applications of Propylene Carbonate as a Solvent in Sustainable Organic Synthesis

ChemSusChem, Volume 19, Issue 17, 14 September 2026.
This review evaluates propylene carbonate (PC) as a non‐toxic green solvent in organic synthesis, highlighting its performance in key reactions including cross‐couplings, asymmetric hydrogenations, peptide synthesis and biocatalysis. Across these processes, PC delivers yields comparable to conventional and alternative green solvents.
Laura G. Aguilar‐Sanchez, Christopher R. Jones   +1 more
wiley   +1 more source

Pericyclic Umpolung in a Catalytic Asymmetric Diels-Alder Reaction of Tropone with Enol Ethers. [PDF]

J Am Chem Soc
Zheng T, Wang Z, Mitschke B, Nöthling N, Leutzsch M, Neese F, List B.   +6 more
europepmc   +1 more source

Catalytic Generation of Cationic Gold Carbene Complexes From 7‐Alkynylnorbornadienes and Their Intermolecular Cyclopropanation With Alkenes

Chemistry – A European Journal, Volume 32, Issue 34, 11 September 2026.
Efficient cationic gold(I)‐catalyzed intermolecular cyclopropanation of 7‐alkynylnorbornadiene derivatives has been developed. This methodology offers the synthesis of a new class of norbornene derivatives in high yield with excellent diastereoselectivity.
Kento Ishida, Kenta Toei, Fumiaki Tomi, Norio Sakai   +3 more
wiley   +1 more source

Development of a Vinylated Cyclic Allene: A Fleeting Strained Diene for the Diels-Alder Reaction. [PDF]

Angew Chem Int Ed Engl
Mizoguchi H, Obata T, Hirai T, Komatsu M, Sakakura A.   +4 more
europepmc   +1 more source

Precision Chemistry for Protein Lysine Modification

Chemistry – A European Journal, Volume 32, Issue 34, 11 September 2026.
Selective modification of lysine residues is challenging due to their similar intrinsic reactivity. Inspired by enzymatic recognition, ligand‐guided electrophiles enable site‐selective labeling and functionalization, while ligand‐guided catalyses achieve regioselective installation of bio‐relevant post‐translational modifications.
Mayu Onoda, Motomu Kanai
wiley   +1 more source

Catalytic Enantioselective Diels-Alder Reaction of Dienes with Acyclic and α,β- and β,β-Disubstituted Enones. [PDF]

J Am Chem Soc
Samsonowicz-Górski J, Ghosh S, Tsuji N, Leutzsch M, Breitenbruch G, Nöthling N, Kraft P, List B.   +7 more
europepmc   +1 more source

Reactivity and Stereoselectivity in the Inverse-Electron-Demand Diels-Alder Reaction of 1-Aza-1,3-Butadiene. [PDF]

Molecules
Sakata K, Go Y, Yoshikawa T.
europepmc   +1 more source