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European Journal of Organic Chemistry, ISSN 1434-193X, 09/2019, Volume 2019, Issue 31-32, pp. 5549 - 5556
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2016, Volume 14, Issue 48, pp. 11438 - 11445
Regio- and stereo- selective reduction of substituted 1,3-aryldiketones, investigated in the presence of different whole cell microorganisms, was found to... 
6556 GROWING CELLS | SUBSTITUTED OXETANES | ANALOGS | KLUYVEROMYCES-MARXIANUS | DRUG DISCOVERY | ENANTIOSELECTIVE REDUCTION | CHEMISTRY, ORGANIC | SUGARS | 3-OXO ESTER REDUCTION | ACCESS | STRATEGIES
Journal Article
Tetrahedron, ISSN 0040-4020, 06/2016, Volume 72, Issue 26, pp. 3641 - 3646
A 4-pot telescoped procedure to prepare oxetane-3-carboxaldehyde and methyl oxetane-3-carboxylate was developed using readily available starting materials.... 
Allylic hydrogenolysis | Homologation | Oxetane | Oxidative cleavage | SUBSTITUTED OXETANES | BUILDING-BLOCKS | DRUG DISCOVERY | OZONOLYSIS | CHEMISTRY, ORGANIC | WITTIG REACTION | RING | ESTERS | INHIBITORS | EFFICIENT | Specialty chemicals industry | Hydrogenation | Synthesis | Acidic oxides | Hydrogenolysis | Tetrahedrons | Homology | Cleavage | Acetates | Rings (mathematics)
Journal Article
Chemical Communications, ISSN 1359-7345, 2018, Volume 54, Issue 80, pp. 11340 - 11343
The development of the highly active pincer-type rhodium catalyst 2 for the nucleophilic Meinwald rearrangement of functionalised terminal epoxides into methyl... 
CATALYZED-REARRANGEMENT | MECHANISM | 2-NICKELA(II)OXETANES | ISOMERIZATION | SUBSTITUTED BENZYLIC ALDEHYDES | REACTIVITY | SELECTIVE SYNTHESIS | CARBONYL REARRANGEMENT | OXIDATIVE ADDITION | CHEMISTRY, MULTIDISCIPLINARY | PROMOTED REARRANGEMENT
Journal Article
CHEMICAL SCIENCE, ISSN 2041-6520, 07/2019, Volume 10, Issue 26, pp. 6531 - 6538
Phenones with elongated chains are shown to be excellent substrates for ligand-promoted asymmetric Grignard synthesis of tertiary alcohols. In turn this... 
ASYMMETRIC-SYNTHESIS | TERTIARY ALCOHOLS | RING EXPANSION | STEREOSELECTIVE-SYNTHESIS | OXIDATIVE CYCLIZATION | CYCLIC ETHERS | SUBSTITUTED TETRAHYDROFURANS | CHEMISTRY, MULTIDISCIPLINARY | 3+2 CYCLOADDITION | GAMMA-BUTYROLACTONES | VINYL OXETANES
Journal Article
Chemical Science, ISSN 2041-6520, 2017, Volume 8, Issue 4, pp. 3002 - 3006
An efficient and convenient synthesis of highly functionalized dihydropyrans has been achieved through rhodium(I)-catalysed tandem C(sp(3))-C(sp(3)) bond... 
TERT-CYCLOBUTANOLS | QUATERNARY STEREOGENIC CENTERS | PRACTICAL SYNTHESIS | ENANTIOSELECTIVE SYNTHESIS | CYCLIZATION REACTIONS | SUBSTITUTED OXETANES | C-C BOND | CARBON-CARBON BONDS | ASYMMETRIC HYDROGENATION | CHEMISTRY, MULTIDISCIPLINARY | MARINE SPONGE
Journal Article
Organic & biomolecular chemistry, ISSN 1477-0520, 12/2016, Volume 14, Issue 48, pp. 11438 - 11445
Regio- and stereo-selective reduction of substituted 1,3-aryldiketones, investigated in the presence of different whole cell microorganisms, was found to... 
Lactobacillus reuteri - metabolism | Saccharomyces cerevisiae - metabolism | Enzymes | Kluyveromyces - cytology | Kluyveromyces - metabolism | Ethers, Cyclic - chemistry | Stereoisomerism | Ethers, Cyclic - metabolism
Journal Article
Chemical Science, ISSN 2041-6520, 03/2017, Volume 8, Issue 4, pp. 3002 - 3006
An efficient and convenient synthesis of highly functionalized dihydropyrans has been achieved through rhodium(i)-catalysed tandem C(sp3)-C(sp3) bond cleavage... 
Organic chemistry | Cycloaddition | Synthesis | Chemical bonds | Chemical reactions | Ligands | Cleavage | Alkynes
Journal Article
Journal of Physical Organic Chemistry, ISSN 0894-3230, 04/2017, Volume 30, Issue 4, p. n/a
The purpose of this study was to explore regioselectivity and stereoselectivity in the Paternò–Büchi reaction of pyrrole derivatives. The regioselective... 
diradical | Photo‐Aldol reaction | oxetanes | Paternò–Büchi reaction | Photo-Aldol reaction | PYRROLE | CHEMISTRY, ORGANIC | CHEMISTRY, PHYSICAL | ADDUCTS | REGIOSELECTIVITY | SUBSTITUTED FURANS | DENSITY | PHOTOADDITION | Paterno Buchi reaction | BENZOPHENONE
Journal Article
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, ISSN 1860-5397, 04/2019, Volume 15, Issue 1, pp. 976 - 980
A catalyst-free novel and efficient methodology for the challenging synthesis of benzo-oxetes from 2'-hydroxyacetophenones mediated by sulfuryl fluoride... 
ASYMMETRIC-SYNTHESIS | benzo-oxetes | ONE-POT SYNTHESIS | SUBSTITUTED OXETANES | DRUG DISCOVERY | 2 '-hydroxyacetophenones | CHEMISTRY, ORGANIC | POLYMERIZATION | FLUORIDE | REDUCTION | sulfuryl fluoride | PHENOLS | RING | Sulfuryl fluoride | Chemistry | Transformation | Fluoride | Fluorides | Pharmaceutical sciences | 2'-hydroxyacetophenones
Journal Article
Organic Letters, ISSN 1523-7060, 06/2015, Volume 17, Issue 11, pp. 2634 - 2637
Journal Article
Tetrahedron, ISSN 0040-4020, 2002, Volume 58, Issue 35, pp. 7065 - 7074
Oxetanes having both a carbonyl functional group and a phenyl group at the 3-position bring about unusual cyclodimerization under the influence of... 
dimerization | oxetanes | epoxides | carbonyl compounds | Carbonyl compounds | Oxetanes | Epoxides | Dimerization | 3-PHENYL-3-(PHTHALIMIDOMETHYL)OXETANE | SUBSTITUTED OXETANES | COMPOSITE RESINS | MONOMER-ISOMERIZATION POLYMERIZATION | CHEMISTRY, ORGANIC | DERIVATIVES
Journal Article
Propellants, Explosives, Pyrotechnics, ISSN 0721-3115, 10/2017, Volume 42, Issue 10, pp. 1143 - 1148
Journal Article
Organic Letters, ISSN 1523-7060, 11/2007, Volume 9, Issue 23, pp. 4681 - 4684
Complex aza-fuzed tricyclic lactones are obtained in a two-step photochemical cycloaddition/acid-catalyzed rearrangement of simple alkoxy maleimide... 
EPOXIDES | KETONES | REAGENTS | ENOL ETHERS | BORON-TRIFLUORIDE ETHERATE | CHEMISTRY, ORGANIC | GENERATION | PATERNO-BUCHI REACTION | PHOTOLYSIS | OXETANES | SUBSTITUTED MALEIMIDES | Ethers, Cyclic - chemical synthesis | Ethers, Cyclic - chemistry | Acids - chemistry | Models, Molecular | Crystallography, X-Ray | Molecular Structure | Catalysis | Alkylation
Journal Article
Tetrahedron, ISSN 0040-4020, 2002, Volume 58, Issue 35, pp. 7049 - 7064
Oxiranes (epoxides) and oxetanes having a carbonyl functional group are chemoselectively isomerized to different heterocyclic compounds via Lewis acid-promoted... 
oxetanes | epoxides | isomerization | carbonyl compounds | Carbonyl compounds | Oxetanes | Epoxides | Isomerization | MAIN-CHAIN | SUBSTITUTED OXETANES | LEWIS-ACID | COMPOSITE RESINS | LIVING POLYMERIZATION | CHEMISTRY, ORGANIC | METHACRYLATE | NEIGHBORING GROUP PARTICIPATION | ORTHO ESTER | RING-OPENING POLYMERIZATION | BICYCLIC AMIDE ACETALS
Journal Article