The cis‐2,3‐bis(trifluoromethyl)cyclopropyl chemotype is introduced. The steric demand of this motif is intermediate between that of the heptafluoroisopropyl and prefluorotertbutyl groups; yet, it induces significantly less lipophilicity than these due to its facial polarity.
Daniel Gaviña +5 more
wiley +1 more source
The electrophilicities (Mayr E) of the α, β‐unsaturated ketones A and B were determined by kinetic studies of their reactions with carbanions (reference nucleophiles) in DMSO at 20°C. The different reactivities of A and B were rationalized by DFT calculations.
Christoph Gross +5 more
wiley +1 more source
Cyclopropenes in Photochemical Reactions
The photochemical side of cyclopropenes. Cyclopropenes are valuable synthetic tools in organic chemistry. In particular, this review focuses on the photochemistry of cyclopropenes. The reactivity of cyclopropenes excited by irradiation is discussed showing their unique potential for organic synthesis.
David Suárez‐García +2 more
wiley +1 more source
Regioselective C3-H Alkylation of Imidazopyridines with Donor-Acceptor Cyclopropanes. [PDF]
Dalkilic O +3 more
europepmc +1 more source
Donor-Acceptor Cyclopropanes: Activation Enabled by a Single, Vinylogous Acceptor. [PDF]
Ahlburg NL +3 more
europepmc +1 more source
(4+3) Annulation of Donor-Acceptor Cyclopropanes and Azadienes: Highly Stereoselective Synthesis of Azepanones. [PDF]
Nicolai S, Waser J.
europepmc +1 more source
Enantioselective (8+3) Cycloadditions by Activation of Donor-Acceptor Cyclopropanes Employing Chiral Brønsted Base Catalysis. [PDF]
McLeod DA +5 more
europepmc +1 more source
Synthesis of Carbazoles and Dihydrocarbazoles by a Divergent Cascade Reaction of Donor-Acceptor Cyclopropanes. [PDF]
Faltracco M, Damian M, Ruijter E.
europepmc +1 more source
Asymmetric ring-opening reactions of donor-acceptor cyclopropanes with 1,3-cyclodiones. [PDF]
Zhang D +5 more
europepmc +1 more source
Lewis-Acid-Catalyzed (3+2)-Cycloadditions of Donor-Acceptor Cyclopropanes with Thioketenes. [PDF]
Mlostoń G +4 more
europepmc +1 more source

