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Rules for ring closure: ring formation by conjugate addition of oxygen nucleophiles
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inferred← citeshttps://doi.org/10.1016/j.carres.2021.108452openalex-snapshot
A general and concise stereodivergent chiral pool approach toward trans-(4S,5R)- and cis-(4R,5R)-5-alkyl-4-methyl-γ-butyrolactones: Syntheses of (+)-trans- and (+)-cis-whisky and cognac lactones from d-(+)-mannitol
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.11.039openalex-snapshot
Diverse synthesis of the C ring fragment of bryostatins via Zn/Cu-promoted conjugate addition of α-hydroxy iodide with enone
inferred← citeshttps://doi.org/10.1016/j.comptc.2012.11.009openalex-snapshot
Intramolecular cyclization reaction mechanism and regioselectivities of unsubstituted and benzene-substituted 4-penteniminyl radicals: A DFT investigation
inferred← citeshttps://doi.org/10.1016/j.foodchem.2018.12.072openalex-snapshot
Comparative study of different cocoa (Theobroma cacao L.) clones in terms of their phytoprostanes and phytofurans contents
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2004.01.004openalex-snapshot
Ring-fluorinated naphthalene and indene synthesis via 6- and 5-endo-trig cyclizations of gem-difluoroalkenes by carbon nucleophiles
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2005.12.023openalex-snapshot
Heck-type 5-endo-trig cyclizations promoted by vinylic fluorines: Ring-fluorinated indene and 3H-pyrrole syntheses from 1,1-difluoro-1-alkenes
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2006.03.006openalex-snapshot
Experimental and theoretical studies on the transannular cyclizations of 3,7-dimethylenebicyclo[3.3.1]nonane with polyfluoroalkyl radicals
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2014.03.009openalex-snapshot
Synthesis of 5-alkyl-3,4-difluorofuran-2(5H)-ones by lactonisation. Effects of substituents on cyclisation ability of fluorinated 4-hydroxyalkanoates. DFT calculations of the cyclisation energies
inferred← citeshttps://doi.org/10.1016/j.plipres.2017.09.004openalex-snapshot
Isoprostanes, neuroprostanes and phytoprostanes: An overview of 25 years of research in chemistry and biology
inferred← citeshttps://doi.org/10.1016/j.tet.2005.06.074openalex-snapshot
An unusual substitution reaction directed by an intramolecular re-arrangement
inferred← citeshttps://doi.org/10.1016/j.tet.2006.09.049openalex-snapshot
Formation of five- and six-membered heterocyclic rings under radical cyclisation conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2007.01.004openalex-snapshot
O→C rearrangements: a powerful strategy for the synthesis of functionalised carbocycles
inferred← citeshttps://doi.org/10.1016/j.tet.2007.10.072openalex-snapshot
The influence of electronic factors on palladium-mediated cycloisomerization: a systematic investigation of competitive 5-exo-dig versus 6-endo-dig cyclizations of sugar alkynols
inferred← citeshttps://doi.org/10.1016/j.tet.2009.09.071openalex-snapshot
The influence of electronic factors on Pd-mediated cycloisomerization: a systematic investigation of competitive 6-exo-dig versus 7-endo-dig cyclizations of sugar alkynols
inferred← citeshttps://doi.org/10.1016/j.tet.2010.04.101openalex-snapshot
A straightforward double intramolecular cyclization of dibenzyl dichalcogenols into a triple bond
inferred← citeshttps://doi.org/10.1016/j.tet.2010.12.055openalex-snapshot
A novel multicomponent approach to the synthesis of 1,3-thiazolidine-2-thiones
inferred← citeshttps://doi.org/10.1016/j.tet.2011.03.091openalex-snapshot
Synthesis of aza-aromatic hydroxylamine-O-sulfonates and their application to tandem nucleophilic addition–electrophilic 5-endo-trig cyclization
inferred← citeshttps://doi.org/10.1016/j.tet.2011.07.073openalex-snapshot
A bioinspired look at the glucosinolate metabolic pathway. Structural insights into the reaction of benzyl isothiocyanate and d-glucosamine
inferred← citeshttps://doi.org/10.1016/j.tet.2011.09.063openalex-snapshot
Regioselective synthesis of flavone derivatives via DMAP-catalyzed cyclization of o-alkynoylphenols
inferred← citeshttps://doi.org/10.1016/j.tet.2011.10.050openalex-snapshot
Parikh–Doering oxidation–dehydration–Ugi cyclization cascade in the development of lactams from formidoalkanols (3>chain length>7)
inferred← citeshttps://doi.org/10.1016/j.tet.2012.12.045openalex-snapshot
Metal-mediated alkynediol cycloisomerization: first and second generation formal total syntheses of didemniserinolipid B
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.008openalex-snapshot
α-Amino acid derived enaminones and their application in the synthesis of N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates and other heterocycles
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.035openalex-snapshot
MCRs reshaped into a switchable microwave-assisted protocol toward 5-aminoimidazoles and dihydrotriazines
inferred← citeshttps://doi.org/10.1016/j.tet.2016.02.039openalex-snapshot
Formation of 2,2-dimethylchroman-4-ones during the photoinduced rearrangement of some aryl 3-methyl-2-butenoate esters. A mechanistic insight
inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.02.009openalex-snapshot
Formal total synthesis of aspergillides A and B
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.11.001openalex-snapshot
A convenient chiron approach to (4R,5R)-5-hydroxyalkylbutan-4-olides and the corresponding 7-oxa analogues from d-(+)-mannitol via an advanced common precursor: syntheses of (−)-muricatacin, 7-oxa-(−)-muricatacin, (4R,5R)-(−)-5-hydroxy-4-decanolide, and (4R,5R)-(−)-7-oxa-5-hydroxy-4-dodecanolide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.05.009openalex-snapshot
Anti-Markovnikov addition to alkenes with a neighbouring thioacetal function
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.11.116openalex-snapshot
An assessment of late transition metals as hydroamination catalysts in the cyclization of C-propargyl vinylogous amides into pyrroles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.04.049openalex-snapshot
BF3-promoted synthesis of spiroindenyl heterocycles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.06.063openalex-snapshot
A mild and convenient one-pot photochemical synthesis of chroman-4-one derivatives. The photo-Fries rearrangement of (hetero)aryl 3-methyl-2-butenoate esters under basic catalysis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.09.049openalex-snapshot
Stereocontrolled construction of tetrasubstituted tetrahydrofurans: synthesis of 2,5-anhydro d-glucitol
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.06.060openalex-snapshot
Silver(I) and gold(I)-promoted synthesis of alkylidene lactones and 2H-chromenes from salicylic and anthranilic acid derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.06.081openalex-snapshot
Expeditious photochemical reaction toward the preparation of substituted chroman-4-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.06.098openalex-snapshot
Metal-free 5-exo-dig cyclization of propargyl urea using TBAF
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.11.023openalex-snapshot
A convenient synthesis of 3,4-cis-disubstituted pyrrolidin-2-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.03.006openalex-snapshot
An efficient oxidative conversion of 2-aryl-2H-chromenes to the corresponding flavones by tert-butylhydroperoxide and copper bromide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.08.041openalex-snapshot
Recent developments in total syntheses of aculeatins
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.10.005openalex-snapshot
Bismuth(III) triflate catalyzed tandem esterification–Fries–oxa-Michael route to 4-chromanones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.04.017openalex-snapshot
Brønsted acid-catalyzed radical C H functionalization of acetone with N-allyl anilines to give 3-(3-oxobutyl)indolines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152367openalex-snapshot
Attempted synthesis of central furopyran core of Diocollettines A via a Gold-Catalyzed cascade 1,6-Diyne cycloisomerization process
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154605openalex-snapshot
Alkylthialactonization: A novel protocol for access to either diastereoisomer of α-(thiomethyl)-γ-butyrolactones
inferred← citeshttps://doi.org/10.1016/j.toxicon.2009.09.001openalex-snapshot
Biosynthesis of toxic naturally-occurring seafood contaminants
inferred← citeshttps://doi.org/10.1016/s0008-6215(98)00063-9openalex-snapshot
Regio- and stereoselective introduction of ether-linked carboxylic side chains into carbohydrates by conjugate addition reactions
inferred← citeshttps://doi.org/10.1016/s0022-0728(01)00367-9openalex-snapshot
Electroreduction of β-hydroxy phenyl sulfones in acetonitrile
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)00818-4openalex-snapshot
Synthesis of silacycloalkenes and silaspirenes by Ru(II)-catalyzed ring-closing metathesis reactions
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00991-7openalex-snapshot
Cyclization reactions of 2-alkynylbenzyl alcohol and 2-alkynylbenzylamine derivatives promoted by tetrabutylammonium fluoride
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)80570-6openalex-snapshot
Aromatic aldehyde methylhydrazones and nitrile oxide. Crystal structure of 3,6-dipenyl-4-methyl-4-methyl-6H-1,2,4,5-oxatriazine.
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)82030-5openalex-snapshot
Formation of orthoesters in the sharpless asymmetric epoxidation : hemisynthesis of labdanes
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)85425-9openalex-snapshot
A versatile regio- and stereospecific annulation method - III.
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)86043-9openalex-snapshot
X=Y-ZH systems as potential 1,3-dipoles
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)86522-4openalex-snapshot
Two lactone formation reactions from 1,3-dioxin-4-ones having hydroxyalkyl group at the 6-position: Difference in ring opening and closure
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)87355-5openalex-snapshot
Anionic activation by fluoride ion in solid-liquid systems
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)87427-5openalex-snapshot
Interconversion of hetidine- and atisine-type diterpenoid alkaloids: facile cleavage and regeneration the c(14)-c(20) bond
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)88335-6openalex-snapshot
Spiroforskolin: Structure and mode of formation
inferred← citeshttps://doi.org/10.1016/s0040-4020(03)00073-5openalex-snapshot
Synthesis of polyfunctional indoles and related heterocycles mediated by cesium and potassium bases
inferred← citeshttps://doi.org/10.1016/s0040-4020(96)00349-3openalex-snapshot
Evidence for cyclic bromonium ion transfer in electrophilic bromination of alkenes: Reaction of ω-alkenyl glycosides with aqueous N-bromosuccinimide
inferred← citeshttps://doi.org/10.1016/s0040-4020(96)00998-2openalex-snapshot
Stereoselective synthesis of five and/or six membered ring hydroxylactones obtained by Lewis acid mediated reaction of γ,δ-epoxy-β-hydroxyesters; access to 5-methylated 2-deoxysugars.
inferred← citeshttps://doi.org/10.1016/s0040-4020(99)00174-xopenalex-snapshot
Lactonisation and lactone ether formation of nerol geraniol compounds. Use of 13C to identify the cyclisation process
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)00037-xopenalex-snapshot
A novel synthetic approach to benzo[h]chromones via sequential intramolecular alkynoyl transfer followed by 6-endo ring closure
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)74401-7openalex-snapshot
Synthetic studies towards batrachotoxin 2. Formation of the oxazepane ring system via a Michael reaction
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)74411-xopenalex-snapshot
Novel approach to the synthesis of chiral oxacyles via ring closure of sugar-derived vinyl sulfones
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)74551-5openalex-snapshot
Synthesis of functionalized tetrahydrofurans
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)81427-6openalex-snapshot
Synthetic studies of 1,7-dioxaspiro[5.5]undecan-4-ones
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)84792-9openalex-snapshot
Total synthesis of (±)-isoavenaciolide and (±)-avenaciolide
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)85236-3openalex-snapshot
Intramolecular Michael addition of cyclic β-ketoester on conjugated acetylenic ketone.
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)88041-7openalex-snapshot
Stereoelectronic effects in ring closure reactions
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)88929-7openalex-snapshot
5-Endo-Trigonal ring closures of unsaturated sulfones.
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