Results 31 to 40 of about 5,434 (218)

Pyrrolidinodiones in Enol-Ugi, Enol-Passerini, and Anomalous Enol-Passerini Condensations

Proceedings, 2019
In continuation of our recent research on the development of novel multicomponent reactions with isocyanides, we have used, for the first time, enols as the acid components in Ugi- and Passerini-type reactions. Thus, electron-poor pyrrolidinodiones react
Ana G. Neo, Carlos F. Marcos
doaj   +1 more source

Cyclization of Activated Methylene Isocyanides with Methyl N(N),N′-Di(tri)substituted Carbamimidothioate: A Novel Entry for the Synthesis of N,1-Aryl-4-tosyl/ethoxycarbonyl-1H-imidazol-5-amines

SynOpen, 2019
Base-induced cyclization of active methylene isocyanides with carbamimidothioates for the synthesis of N,1-aryl-4-tosyl/ethylcarboxy-1H-imidazol-5-amines is reported.
Dukanya Dukanya, Toreshettahally R. Swaroop, Shobith Rangappa, Kanchugarakoppal S. Rangappa, Basappa Basappa   +4 more
doaj   +1 more source

Multicomponent Reactions of Isocyanides for the Preparation of Low Molecular Weight Gelators: Preliminary Studies

Chemistry Proceedings, 2021
Low molecular weight gelators, LMWGs, are small molecules that can self-associate in organic solvents or in water to form fibrous supramolecular architectures and three-dimensional networks that present important applications in several fields.
José L. Ramiro, Carlos F. Marcos, Ana G. Neo   +2 more
doaj   +1 more source

PHOTOCHEMICAL OXIDATION AND ISOMERIZATION OF ISOCYANIDES.

, 1973
PHOTOCHEMICAL OXIDATION AND ISOMERIZATION OF ...
ANTHONY JACOB JR. SPAK (7964411)
core   +3 more sources

Site‐Specific Protein Bioconjugation Through Cellular Incorporation of Noncanonical Amino Acids

Angewandte Chemie, EarlyView.
Genetic code expansion (GCE) enables site‐specific installation of noncanonical amino acids containing bioorthogonal conjugation handles, allowing precise, homogeneous protein modification. This review examines the principles of orthogonal translation, surveys the chemistries available for chemoselective labeling, and highlights emerging multi‐site ...
Rahul Sarkar, Manas Joshi, Abhishek Chatterjee   +2 more
wiley   +2 more sources

Macrocyclization of ω‐Isocyano Aldehydes

Angewandte Chemie, EarlyView.
The ω‐isocyano aldehydes readily undergo cyclization to afford α‐acyloxy, α‐hydroxy, α‐acetamido, and α‐keto macrolactams, as well as tetrazole‐fused macrocycles, via C(sp3)─C(sp2) bond formation, providing access to diverse α‐functionalized medium‐sized lactams and macrolactams. ABSTRACT Medium‐sized rings and macrocycles constitute a privileged class
Baochao Yang, Teerawat Songsichan, Cyril Piemontesi, Qian Wang, Jieping Zhu   +4 more
wiley   +2 more sources

HETEROCYCLES FROM BIARYL ISOCYANIDES: PHENYLNAPHTHYL AND NAPHTHYLPHENYL SYSTEMS.

, 1977
HETEROCYCLES FROM BIARYL ISOCYANIDES: PHENYLNAPHTHYL AND NAPHTHYLPHENYL ...
JAYANTIBHAI R. PATEL (7986260)
core   +3 more sources

Biosynthetic Routes to Natural Isocyanides

, 2020
International audienceAs intriguing as it may appear, natural products bearing an isocyanide function are well known in different kingdoms of living organisms.
Evanno, Laurent, Poupon, Erwan, Laurent Evanno, Erwan Poupon, Xinming Zhang, Zhang, Xinming   +5 more
core   +1 more source

First Homoleptic Isocyanides of Niobium and Tantalum¹

, 2016
First Homoleptic Isocyanides of Niobium and ...
John E. Ellis (2053192), Victor G. Young (1405513), Mikhail V. Barybin (1483429)   +2 more
core   +2 more sources

Efficacy of radical reactions of isocyanides with heteroatom radicals in organic synthesis

Beilstein Journal of Organic Chemistry
Isocyanide is a promising synthetic reagent not only as a one-carbon homologation reagent but also as a nitrogen source for nitrogen-containing molecules.
Akiya Ogawa, Yuki Yamamoto
doaj   +1 more source