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Enumeration of Ring–Chain Tautomers Based on SMIRKS Rules

https://doi.org/10.1021/ci500363p
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/chem.201200363openalex-snapshot
Solvent‐Catalyzed Ring–Chain–Ring Tautomerization in Axially Chiral Compounds
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Recent Developments in the Ring‐Chain Tautomerism of 1,3‐Heterocycles
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Study of the Substituent‐Influenced Anomeric Effect in the Ring‐Chain Tautomerism of 1‐Alkyl‐3‐aryl‐naphth[1,2‐e][1,3]oxazines
inferredcites →https://doi.org/10.1002/ejoc.200600974openalex-snapshot
Ring–Chain Tautomerism of Simplified Analogues of Isoniazid–NAD(P) Adducts: an Experimental and Theoretical Study
inferredcites →https://doi.org/10.1002/jcc.540150802openalex-snapshot
Hash codes for the identification and classification of molecular structure elements
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Crystal structural determination of ring‐chain tautomers of 1,2,3,4‐tetrahydro‐s‐tetrazines
inferredcites →https://doi.org/10.1002/jlcr.1787openalex-snapshot
Ring‐chain tautomerism in 2,2‐bis(2‐thienyl)tetrahydrofurans: preparation of [butene‐2H5]‐tiagabine
inferredcites →https://doi.org/10.1002/jmr.1058openalex-snapshot
Warfarin: an environment‐dependent switchable molecular probe
inferredcites →https://doi.org/10.1002/rcm.3528openalex-snapshot
Substituent effects on the ring‐chain tautomerism of some 1,3‐oxazolidine derivatives
inferredcites →https://doi.org/10.1007/s10593-013-1287-0openalex-snapshot
Ring-chain tautomerism of 2-aryl-6-oxohexahydropyrimidine-4-carboxylic acid sodium salts
inferredcites →https://doi.org/10.1007/s10822-009-9303-2openalex-snapshot
Let’s not forget tautomers
inferredcites →https://doi.org/10.1007/s10822-010-9329-5openalex-snapshot
So you think you understand tautomerism?
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Warfarin: history, tautomerism and activity
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Tautomerism in chemical information management systems
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Tautomerism in large databases
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Tautomerism in drug discovery
inferredcites →https://doi.org/10.1007/s11172-006-0549-8openalex-snapshot
Silylation of bicyclic six-membered nitronates. Ring—chain tautomerism of intermediate N,N bis(oxy)iminium cations
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Reactions of (E)-3,3,3-trichloro(trifluoro)-1-nitropropenes with enamines derived from cycloalkanones. A new type of ring-chain tautomerism in a series of cyclobutane derivatives and stereochemistry of the products
inferredcites →https://doi.org/10.1007/s11172-012-0264-6openalex-snapshot
1,4-Conjugate addition of 2-hydroxynaphthazarins to acyclic and cyclic α,β-unsaturated ketones. Prototropic ring-chain tautomerism of the adducts
inferredcites →https://doi.org/10.1016/0040-4020(80)80067-6openalex-snapshot
Recent developments in the synthesis, structure and chemistry of bridgehead alkenes
inferredcites →https://doi.org/10.1016/j.molstruc.2011.09.014openalex-snapshot
Intramolecular interactions in dimedone and phenalen-1,3-dione adducts of 2(4)-pyridinecarboxaldehyde: Enol–enol and ring-chain tautomerism, strong hydrogen bonding, zwitterions
inferredcites →https://doi.org/10.1016/j.tet.2005.04.074openalex-snapshot
A comparison of ring-chain tautomerism in heterocycles derived from 2-aminobenzenesulfonamide and anthranilamide
inferredcites →https://doi.org/10.1016/j.tetasy.2011.11.011openalex-snapshot
Substituent effects in ring-chain tautomerism of the condensation products of non-racemic 1,2-aminoalcohols with aromatic aldehydes
inferredcites →https://doi.org/10.1016/j.tetlet.2009.03.201openalex-snapshot
An imidazolidin-1-ol, nitrone and oxadiazinane ring-chain-ring tautomeric dynamic combinatorial library
inferredcites →https://doi.org/10.1016/j.tetlet.2011.04.013openalex-snapshot
Unusual ring-chain tautomerism in bicyclo[4.2.0]octane derivatives
inferredcites →https://doi.org/10.1016/s0040-4020(03)00331-4openalex-snapshot
Substituent effects in the ring-chain tautomerism of 1,3-diaryl-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazines
inferredcites →https://doi.org/10.1016/s0065-2725(08)60304-9openalex-snapshot
Recent Developments in Ring-Chain Tautomerism II. Intramolecular Reversible Addition Reactions to the C=N, C=N, C=C, and C=C Groups
inferredcites →https://doi.org/10.1016/s0065-2725(16)30049-6openalex-snapshot
Advances in Heterocyclic chemistry
inferredcites →https://doi.org/10.1016/s0926-2040(03)00029-8openalex-snapshot
Ring-chain tautomerism in solid-phase erythromycin A: evidence by solid-state NMR
inferredcites →https://doi.org/10.1021/ci025582dopenalex-snapshot
Advanced Exact Structure Searching in Large Databases of Chemical Compounds
inferredcites →https://doi.org/10.1021/ci060109bopenalex-snapshot
The Impact of Tautomer Forms on Pharmacophore-Based Virtual Screening
inferredcites →https://doi.org/10.1021/ci800340jopenalex-snapshot
Tautomer Enumeration and Stability Prediction for Virtual Screening on Large Chemical Databases
inferredcites →https://doi.org/10.1021/jm00221a025openalex-snapshot
Structure of warfarin in solution
inferredcites →https://doi.org/10.1021/jm049838dopenalex-snapshot
CHMIS-C: A Comprehensive Herbal Medicine Information System for Cancer
inferredcites →https://doi.org/10.1021/jo00226a018openalex-snapshot
Ring-chain tautomerism in 1,3-oxazines
inferredcites →https://doi.org/10.1021/jo01285a077openalex-snapshot
Ring-chain tautomers of 6-substituted 2-acetylbenzoic acids
inferredcites →https://doi.org/10.1021/jo2008498openalex-snapshot
Synthesis and Ring-Chain-Ring Tautomerism of Bisoxazolidines, Thiazolidinyloxazolidines, and Spirothiazolidines
inferredcites →https://doi.org/10.1021/jp072505iopenalex-snapshot
The Spectrophysics of Warfarin: Implications for Protein Binding
inferredcites →https://doi.org/10.1023/a:1015419321855openalex-snapshot
Molecular design of tautomeric interconversions of heterocycles
inferredcites →https://doi.org/10.1023/b:rucb.0000035634.33295.0copenalex-snapshot
New type of ring-chain tautomerism. Direct evidence from 1H NMR spectroscopy
inferredcites →https://doi.org/10.1023/b:rujo.0000010565.77155.abopenalex-snapshot
Synthesis of 2-(1-Alkoxyvinyl)oxazolidines by Condensation of 2-Alkoxypropenals with 2-Aminoalkanols and Ring-Chain Tautomerism of the Products
inferredcites →https://doi.org/10.1039/c2dt11749eopenalex-snapshot
The ring–chain tautomeric equilibria of selenium macrocyclic compounds: the isolation of the ring tautomer
inferredcites →https://doi.org/10.1039/c39760000734openalex-snapshot
Rules for ring closure
inferredcites →https://doi.org/10.1039/ct9150701080openalex-snapshot
CXIX.—The formation and stability of spiro-compounds. Part I. spiro-Compounds from cyclohexane
inferredcites →https://doi.org/10.1070/mc2003v013n06abeh001835openalex-snapshot
New examples of ring–chain tautomeric conversions
inferredcites →https://doi.org/10.1081/rrs-120026975openalex-snapshot
Tautomerism in Computer‐Aided Drug Design
inferredcites →https://doi.org/10.1093/nar/gkt1076openalex-snapshot
Data, information, knowledge and principle: back to metabolism in KEGG
inferredcites →https://doi.org/10.1139/v71-635openalex-snapshot
Ring–Chain Tautomerism of Hydroxyketones
inferredcites →https://doi.org/10.3987/com-02-9469openalex-snapshot
Ring-Chain Tautomerism of Halogenated Phenolphthaleins: Vibrational Spectroscopic and Semiempirical MO Study

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