Results 51 to 60 of about 9,019 (233)
Monosubstituted N‐arylhydroxylamines represent a unique subclass of hydroxylamines that act as pivotal intermediates in redox transformations and as versatile platforms for further synthetic transformations. They serve as key building blocks in the synthesis of architecturally complex heterocycles and other valuable organic compounds.
Michael G. Kallitsakis +2 more
wiley +1 more source
Donor-Acceptor Cyclopropanes with an Amino Group as Donor
Over the last two decades, a renaissance has been witnessed in the research field of donor-acceptor (DA) cyclopropanes. Among all the subclasses of DA cyclopropanes, DA cyclopropanes with an amino group as donor (DA aminocyclopropanes) have drawn ...
Waser, Jerome, Wang, Ming Ming
core +1 more source
Efficient and scalable syntheses of enantiomerically pure (2R,1'S,2'R)- and (2S,1'S,2'R)-3-[2-mono(di,tri)fluoromethylcyclopropyl]alanines 9a–c, as well as allo-D-threonine (4) and (2S,3R)-β-methylphenylalanine (3), using the Belokon' approach with (S ...
Armin de Meijere +5 more
doaj +1 more source
The competitive formation of oxiranes 1 and cyclopropanes 2 in the reaction of 2-halogeno-acrylic acid-derivatives, carbonyl-compounds and bases is discussed.
R. Scheffold +4 more
doaj +1 more source
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 +3 more
wiley +1 more source
Studies on the Diastereoselective Preparation of Bis-cyclopropanes
The identification of two natural products, FR-900848 and U-106305, has stimulated interest concerning the relationship between configurational isomerism, conformational isomerism, and biological activity of polycyclopropanes.
Christopher A. Verbicky (3025374) +2 more
core +2 more sources
Oxidative Generation and Reactivity of the Cyclopropyl Radical From a Martin Silicate
A photoredox strategy employing Martin silicates enables the oxidative generation and controlled capture of cyclopropyl radicals, including the naked one, long considered challenging intermediates. The method affords functionalized cyclopropanes through both Giese‐type additions and dual nickel/photoredox C(sp3)−C(sp2) cross‐couplings.
Amal Lakhal +3 more
wiley +1 more source
New chemistry of donor-acceptor cyclopropanes [PDF]
textDonor-Acceptor (DA) cyclopropanes are considered to be well-understood compounds with predictable chemistry. This dissertation focuses on our recent advances and synthetic applications of DA cyclopropanes principally involving 1,3-dipole ...
Yu, Ming
core
Synthetic Applications of Carbohydrate-derived Donor-Acceptor Cyclopropanes
In this account, we elaborate our group's contribution towards understanding the chemistry of carbohydrate-derived donor-acceptor (DA) cyclopropanes. Our work was mainly focused on the ring opening of these versatile chiral synthons under the influence ...
Sridhar, Perali Ramu +2 more
core +1 more source
Clathrate hydrate crystallization
Abstract Clathrate hydrate crystallization has been an area of interest to chemical engineers from the point of view of crystal structure, thermophysical properties, phase equilibria, kinetics, industrial applications, and environmental (climate change) implications.
Peter Englezos
wiley +1 more source

