Results 141 to 150 of about 2,936 (205)
1,4-Pd Migration-Enabled Synthesis of Fused 4-Membered Rings. [PDF]
Tsitopoulou M +3 more
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Trimorphism of a binary cocrystal system with hydrogen-bonded zig-zag, double helix and quadruple helix structures. [PDF]
Duncan AJE +4 more
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Access to Complex Scaffolds Through [2 + 2] Cycloadditions of Strained Cyclic Allenes. [PDF]
McVeigh MS +3 more
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Facile Synthesis of Housanes by an Unexpected Strategy. [PDF]
Liu Y +7 more
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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.
Tobias Seiser +2 more
exaly +5 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.
Tobias Seiser +2 more
exaly +5 more sources
Infrared and Raman spectra of cyclobutane and cyclobutane-d8
Spectrochimica Acta Part A: Molecular Spectroscopy, 1972Abstract New i.r. and Raman measurements are reported for cyclo butane and cyclo butane- d 8 . They include i.r. spectra on the gas at room temperature and on the solid at about 100°K. Raman spectra have been measured for the gas and liquid at room temperature and for the solid at 113°K. These data allow the assignments (for D 2d ) to be put on
Foil A. Miller +3 more
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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

