Scalable and Green Extraction of Enantiopure Sparteine from Lupinus Species: A Comparative E-Factor Study (ICPSR doi:10.26165/JUELICH-DATA/HIC98E)

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Document Description

Citation

Title:

Scalable and Green Extraction of Enantiopure Sparteine from Lupinus Species: A Comparative E-Factor Study

Identification Number:

doi:10.26165/JUELICH-DATA/HIC98E

Distributor:

Jülich DATA

Date of Distribution:

2026-05-19

Version:

1

Bibliographic Citation:

Sowa, Philipp; Loehrer, Marco; Beers, Ashley; Ophoven, Vera; Henßen, Birgit; Klein, Andreas Sebastian; Pietruszka, Jörg; Classen, Thomas, 2026, "Scalable and Green Extraction of Enantiopure Sparteine from Lupinus Species: A Comparative E-Factor Study", https://doi.org/10.26165/JUELICH-DATA/HIC98E, Jülich DATA, V1

Study Description

Citation

Title:

Scalable and Green Extraction of Enantiopure Sparteine from Lupinus Species: A Comparative E-Factor Study

Identification Number:

doi:10.26165/JUELICH-DATA/HIC98E

Authoring Entity:

Sowa, Philipp (Heinrich-Heine-University Düsseldorf)

Loehrer, Marco (RWTH University Aachen)

Beers, Ashley (Heinrich-Heine-University Düsseldorf)

Ophoven, Vera (Heinrich-Heine-University Düsseldorf)

Henßen, Birgit (Heinrich-Heine-University Düsseldorf, Forschungszentrum Jülich GmbH)

Klein, Andreas Sebastian (Heinrich-Heine-University Düsseldorf)

Pietruszka, Jörg (Heinrich-Heine-University Düsseldorf, Forschungszentrum Jülich GmbH)

Classen, Thomas (Forschungszentrum Jülich GmbH)

Distributor:

Jülich DATA

Access Authority:

Classen, Thomas

Depositor:

Classen, Thomas

Date of Deposit:

2026-05-04

Study Scope

Keywords:

Chemistry, alkaloids, sustainable chemistry, lupin, E-factor, sparteine

Abstract:

<h1>Repository Preface</h1> <p>This repository contains curated chemical data and computational resources for several lupin alkaloids. Below is a summary of the primary compounds, their molecular formulas, sample identifiers (GC‑MS), and SMILES strings.</p> <hr> <h2>Compound Summary</h2> <dl> <dt><b>Name:</b> lupanine</dt> <dd><b>Molecular Formula:</b> C15H24N2O<br> <b>Sample Identifier (GC‑MS):</b> PSO0001_E22 Lupanine<br> <b>SMILES Code:</b> <code>O=C1CCC[C@@]2([H])N1C[C@@H]3C[C@H]2CN4[C@@]3([H])CCCC4</code></dd> <dt><b>Name:</b> sparteine</dt> <dd><b>Molecular Formula:</b> C15H26N2<br> <b>Sample Identifier (GC‑MS):</b> PSO0003_Sparteine<br> <b>SMILES Code:</b> <code>[H][C@@]12N(C[C@@H]3C[C@H]2CN4[C@@]3([H])CCCC4)CCCC1</code></dd> <dt><b>Name:</b> 13α‑hydroxylupanine</dt> <dd><b>Molecular Formula:</b> C15H24N2O2<br> <b>Sample Identifier (GC‑MS):</b> PSO0001_ABE49_13α‑Hydroxylupanine<br> <b>SMILES Code:</b> <code>[H][C@@]12N(C[C@@H]3C[C@H]2CN4[C@@]3([H])C[C@@H](O)CC4)C(CCC1)=O</code></dd> <dt><b>Name:</b> 12,13‑anhydrolupanine</dt> <dd><b>Molecular Formula:</b> C15H22N2O<br> <b>Sample Identifier (GC‑MS):</b> PSO0015_V07 SF 9‑11<br> <b>SMILES Code:</b> <code>O=C1CCCC2N1CC3CC2CN4C3C=CCC4</code></dd> <dt><b>Name:</b> 13,14‑anhydrolupanine</dt> <dd><b>Molecular Formula:</b> C15H22N2O<br> <b>Sample Identifier (GC‑MS):</b> PSO0015_V07 SF 5‑6<br> <b>SMILES Code:</b> <code>O=C1CCCC2N1CC3CC2CN4C3CC=CC4</code></dd> </dl> <hr> <h2>Available Data</h2> <ul> <li>Compound metadata (name, formula, GC‑MS identifier, SMILES) as listed above.</li> <li>Computational foundations for Environmental‑Factors (E+) located in the following folders: <ul> <li>Lupinus_albus</li> <li>Lupinus_angustifolius</li> <li>Lupinus_mutabilis</li> </ul> </li> <li>NMR spectra for the dehydro‑lupanine isomers stored in the <code>NMR</code> folder: <ul> <li>12,13‑dehydrolupanine</li> <li>13,14‑dehydrolupanine</li> </ul> </li> </ul>

Methodology and Processing

Sources Statement

Data Access

Notes:

CC0 Waiver

Other Study Description Materials

Other Study-Related Materials

Label:

2026-05-04_PSO.7z

Notes:

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