On the public citation graph

Polymorphs of a Cocrystal with Achiral and Chiral Structures Prepared by Pseudoseeding: Tryptamine/Hydrocinnamic Acid

0 signed · 49 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1521-3773(19991203)38:23<3418::aid-anie3418>3.0.co;2-vopenalex-snapshot

Absolute Asymmetric Synthesis: The Origin, Control, and Amplification of Chirality

inferredcites →https://doi.org/10.1002/chem.19970030506openalex-snapshot

Absolute Asymmetric Synthesis from Achiral Molecules in the Chiral Crystalline Environment

inferredcites →https://doi.org/10.1016/s0040-4039(97)01072-1openalex-snapshot

Preparation, structure and discrimination of a chiral bimolecular crystal by the self-assembly of 3-indolepropionic acid and phenanthridine

inferredcites →https://doi.org/10.1016/s0957-4166(98)00197-9openalex-snapshot

Chiral crystalline salts from achiral biphenylcarboxylic acids and tryptamine

inferredcites →https://doi.org/10.1021/ar50138a001openalex-snapshot

Asymmetric synthesis via reactions in chiral crystals

inferredcites →https://doi.org/10.1021/ja00086a012openalex-snapshot

An Absolute Asymmetric Synthesis of the [2 + 2] Cycloadduct via Single Crystal-to-Single Crystal Transformation by Charge-Transfer Excitation of Solid-State Molecular Complexes Composed of Arylolefins and Bis[1,2,5]thiadiazolotetracyanoquinodimethane

inferredcites →https://doi.org/10.1021/ja00787a081openalex-snapshot

Reactions in chiral crystals. Optically active heterophotodimer formation from chiral single crystals

inferredcites →https://doi.org/10.1021/ja00787a082openalex-snapshot

General base catalyzed intramolecular transesterification

inferredcites →https://doi.org/10.1021/ja961106qopenalex-snapshot

Generation of Chirality in a Two-Component Molecular Crystal of Acridine and Diphenylacetic Acid and Its Absolute Asymmetric Photodecarboxylating Condensation

inferredcites →https://doi.org/10.1021/jo970719yopenalex-snapshot

Synthesis, Structure, and Discrimination of Chiral Bimolecular Crystals by Using Diphenylacetic Acid and Aza Aromatic Compounds

inferredcites →https://doi.org/10.1021/jo9815195openalex-snapshot

Chiral Bimolecular Crystallization of Tryptamine and Achiral Carboxylic Acids

inferredcites →https://doi.org/10.1021/jo982257+openalex-snapshot

Generation of Chirality in Two-Component Molecular Crystals of Tryptamine and Achiral Carboxylic Acids

inferredcites →https://doi.org/10.1080/10587259608034077openalex-snapshot

Two-Component Mixed Crystals Consisting of Nitroanilines and Nitrophenols and Their Nonlinear Optical Property

inferredcites →https://doi.org/10.1080/10587259608046004openalex-snapshot

Mixed Crystals Containing Methyl-Substituted Nitroanilines and Their Second Harmonic Generation Activity

inferredcites →https://doi.org/10.1080/10610270108034889openalex-snapshot

Helicity Control in the Preparation of Chiral Co-crystals from Tryptamine and Achiral Carboxylic Acids by Pseudo-seeding

inferredcites →https://doi.org/10.1080/10610279908048716openalex-snapshot

Preparation and Structure of Chiral Two-component Molecular Crystals from 3-(3-Indolyl)propanoic Acid and Aza Aromatic Compounds

inferredcites →https://doi.org/10.5059/yukigoseikyokaishi.56.268openalex-snapshot

Chiral Crystallization of Achiral Organic Compounds. Generation of Chirality Without Chiral Environment (Part 1).

inferredcites →https://doi.org/10.5059/yukigoseikyokaishi.56.466openalex-snapshot

Chiral Crystallization of Achiral Organic Compounds. Generation of Chirality without Chiral Environment. (Part 2).

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4693166openalex-extracted

Optical Limiting Activity Of Cytosinium Hydrogen Bromide

inferred← citeshttps://doi.org/10.1002/ange.200301721openalex-snapshot

Reaktionen zwischen und in Molekülkristallen

inferred← citeshttps://doi.org/10.1002/anie.200301721openalex-snapshot

Reactions Between or Within Molecular Crystals

inferred← citeshttps://doi.org/10.1002/chem.200500503openalex-snapshot

Induction and Inhibition of Preferential Enrichment by Controlling the Mode of the Polymorphic Transition with Seed Crystals

inferred← citeshttps://doi.org/10.1002/chem.200701709openalex-snapshot

Topological Classification and Supramolecular Chirality of 21‐Helical Ladder‐Type Hydrogen‐Bond Networks Composed of Primary Ammonium Carboxylates: Bundle Control in 21‐Helical Assemblies

inferred← citeshttps://doi.org/10.1007/s10973-007-8484-yopenalex-snapshot

Mechanical mixing of molecular crystals

inferred← citeshttps://doi.org/10.1007/s11095-008-9554-yopenalex-snapshot

Dissolution Enhancement by Bio-Inspired Mesocrystals: The Study of Racemic (R,S)-(±)-Sodium Ibuprofen Dihydrate

inferred← citeshttps://doi.org/10.1007/s11224-007-9265-8openalex-snapshot

Are there preferable conformations of the tryptammonium cation in the solid state? Crystal structure and solid-state linear polarized IR-spectroscopic study of tryptammonium hydrogentartarate

inferred← citeshttps://doi.org/10.1016/b978-044451669-5/50003-xopenalex-snapshot

Physical properties and enantiomeric composition

inferred← citeshttps://doi.org/10.1016/j.cplett.2016.02.042openalex-snapshot

Protonation-induced change in the conformation, crystal structure and property of triarylmethyl carbocation radical

inferred← citeshttps://doi.org/10.1016/j.ijpharm.2012.10.043openalex-snapshot

Pharmaceutical cocrystals and poorly soluble drugs

inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.07.036openalex-snapshot

Weak interactions in barbituric acid derivatives. Unusually steady intermolecular organic “sandwich” complexes. π–π Stacking versus hydrogen bonding interactions

inferred← citeshttps://doi.org/10.1016/j.molstruc.2014.06.077openalex-snapshot

Seven organic salts assembled from hydrogen-bonds of N–H⋯O, O–H⋯O, and C–H⋯O between acidic compounds and bis(benzimidazole)

inferred← citeshttps://doi.org/10.1016/j.molstruc.2014.12.057openalex-snapshot

Spontaneous resolution in a new chiral purely organic crystal containing homochiral helical chains: Synthesis, crystal structure, and phosphorescence

inferred← citeshttps://doi.org/10.1016/j.tetasy.2011.07.012openalex-snapshot

Hydrogen-bonded helices in 2-aminothiazole derivatives: generation of chiral crystals from small achiral molecules

inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00819openalex-snapshot

Spontaneous Deracemizations

inferred← citeshttps://doi.org/10.1021/cg015542mopenalex-snapshot

Synthesis, Structure, and Second-Harmonic Generation of Noncentrosymmetric Cocrystals of 2-Amino-5-nitropyridine with Achiral Benzenesulfonic Acids

inferred← citeshttps://doi.org/10.1021/cg034187sopenalex-snapshot

Preparation of Cocrystals of 2-Amino-3-nitropyridine with Benzenesulfonic Acids for Second-Order Nonlinear Optical Materials

inferred← citeshttps://doi.org/10.1021/cg200466bopenalex-snapshot

Conformational Diversity of Thiosemicarbazonatovanadium(V) Complexes in the Solid State: From Polymorphism to Isostructurality

inferred← citeshttps://doi.org/10.1021/cg4006357openalex-snapshot

Polymorphic Co-crystals from Polymorphic Co-crystal Formers: Competition between Carboxylic Acid···Pyridine and Phenol···Pyridine Hydrogen Bonds

inferred← citeshttps://doi.org/10.1021/cg901412dopenalex-snapshot

Screening, Manufacturing, Photoluminescence, and Molecular Recognition of Co-Crystals: Cytosine with Dicarboxylic Acids

inferred← citeshttps://doi.org/10.1021/jacs.0c05563openalex-snapshot

Self-Assembly of a Chiral Cubic Three-Connected Net from the High Symmetry Molecules C 60 and SnI 4

inferred← citeshttps://doi.org/10.1039/b504668hopenalex-snapshot

Making crystals from crystals: a green route to crystal engineering and polymorphism

inferred← citeshttps://doi.org/10.1039/b516165gopenalex-snapshot

Mechanochemical preparation of molecular and supramolecular organometallic materials and coordination networks

inferred← citeshttps://doi.org/10.1039/b803866jopenalex-snapshot

Current directions in co-crystal growth

inferred← citeshttps://doi.org/10.1039/b811438bopenalex-snapshot

The crystal structures of chloro and methyl ortho-benzoic acids and their co-crystal: rationalizing similarities and differences

inferred← citeshttps://doi.org/10.1039/c7cc00907kopenalex-snapshot

Reversible crystal-to-crystal chiral resolution: making/breaking non-bonding S⋯O interactions

inferred← citeshttps://doi.org/10.1201/b11197-9openalex-snapshot

References

inferred← citeshttps://doi.org/10.15171/apb.2016.062openalex-snapshot

Pharmaceutical Cocrystals: Regulatory and Strategic Aspects, Design and Development

inferred← citeshttps://doi.org/10.24191/sl.v15i1.11799openalex-snapshot

Preliminary assessment on cocrystals of nicotinamide:cinnamic acid and nicotinamide:p-coumaric acid at different solvents and ratio

inferred← citeshttps://doi.org/10.26434/chemrxiv.12196788.v1openalex-snapshot

A Chiral Van Der Waals Material Self-Assembled from the High Symmetry Molecules C60 and SnI4

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.