Results 151 to 160 of about 4,067 (210)
Triplet Energy Transfer-Mediated Intermolecular Paternò-Büchi Reaction for the Synthesis of Trifluoromethylated Oxetanes. [PDF]
Zhu Y +3 more
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Pyrrolizidine alkaloids – natural toxins risk in Queensland honey [PDF]
Anuj, S. R. +8 more
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Light-Induced Disruption of 1D Wire-Like Arrays of Monoatomic Ag(I) Ions: Single-Crystal Reaction with Crystal Softening. [PDF]
Li C +5 more
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Organo-catalyzed photoelectrochemical ring-contraction of arylidenecyclobutanols via radical cation-triggered semipinacol rearrangement. [PDF]
Zheng Y +5 more
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Photoinduced Transformations with Diverse Maleimide Scaffolds. [PDF]
Parthiban J, Garg D, Sivaguru J.
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Angewandte Chemie - International Edition, 2011
AbstractThe exploitation of ring strain as a driving force to facilitate chemical reactions is a well‐appreciated principle in organic chemistry. The most prominent and most frequently used compound classes in this respect are oxiranes and cyclopropanes.
tanguy saget, Duc N Tran, Nicolai Cramer
exaly +3 more sources
AbstractThe exploitation of ring strain as a driving force to facilitate chemical reactions is a well‐appreciated principle in organic chemistry. The most prominent and most frequently used compound classes in this respect are oxiranes and cyclopropanes.
tanguy saget, Duc N Tran, Nicolai Cramer
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Naturally occurring cyclobutanes
ChemInform, 2001AbstractFor Abstract see ChemInform Abstract in Full Text.
Trond Vidar Hansen, Yngve Stenstrom
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Synthesis of Cyclobutane Nucleosides
Nucleosides, Nucleotides & Nucleic Acids, 20112-(6-Chloropurinyl)-3-benzoyloxymethylcyclobutanone can be prepared by reaction of 6-chloropurine with 3-benzoyloxymethyl-2-bromocyclobutanone. The N-alkylation gave both N-9 and N-7 regioisomers. Both regioisomers upon hydride reduction followed by aminolysis gave the corresponding adenine nucleoside analogues.
Abdelaziz, Ebead +2 more
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Neurochemical Research, 1980
Both cis- and trans-3-aminocyclobutane-1-carboxylic acid have been synthesized as conformationally restricted analogs of GABA. The cis isomer displayed weak to moderate GABA-like activity with respect to (1) inhibition of GABA uptake in rat brain minislices, (2) inhibition of sodium-independent binding of GABA to rat brain membranes, (3) activity as a ...
R D, Allan +6 more
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Both cis- and trans-3-aminocyclobutane-1-carboxylic acid have been synthesized as conformationally restricted analogs of GABA. The cis isomer displayed weak to moderate GABA-like activity with respect to (1) inhibition of GABA uptake in rat brain minislices, (2) inhibition of sodium-independent binding of GABA to rat brain membranes, (3) activity as a ...
R D, Allan +6 more
openaire +2 more sources

