Reference health

Efficient and sustainable transformation of gamma-valerolactone into nylon monomers

https://doi.org/10.1039/c5gc01922b
CiteStamped reference-health badge
28/28 checkable references clean · checked 2026-07-22

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

1 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 28 checked references that resolve
resolves10.1021/cr068360d
Synthesis of Transportation Fuels from Biomass:  Chemistry, Catalysts, and Engineering
resolves10.1021/cr050989d
Chemical Routes for the Transformation of Biomass into Chemicals
resolves10.1039/C3GC41935E
Green and sustainable manufacture of chemicals from biomass: state of the art
resolves10.1039/C1CS15147A
Conversion of biomass to selected chemical products
resolves10.1126/science.1191662
Connecting Biomass and Petroleum Processing with a Chemical Bridge
resolves10.1126/science.1184362
Integrated Catalytic Conversion of γ-Valerolactone to Liquid Alkenes for Transportation Fuels
resolves10.1002/anie.201002061
Pentenoic Acid Pathways for Cellulosic Biofuels
resolves10.1039/B712863K
γ-Valerolactone—a sustainable liquid for energy and carbon-based chemicals
resolves10.1007/s11244-008-9047-6
Integration of Homogeneous and Heterogeneous Catalytic Processes for a Multi-step Conversion of Biomass: From Sucrose to Levulinic Acid, γ-Valerolactone, 1,4-Pentanediol, 2-Methyl-tetrahydrofuran, and Alkanes
resolves10.1002/anie.200902281
Catalytic Conversion of Biomass‐Derived Carbohydrates into γ‐Valerolactone without Using an External H<sub>2</sub> Supply
resolves10.1021/cs501922e
Environmentally Friendly Synthesis of γ-Valerolactone by Direct Catalytic Conversion of Renewable Sources
resolves10.1016/j.apcata.2004.05.048
Catalytic synthesis of α-methylene-γ-valerolactone: a biomass-derived acrylic monomer
resolves10.1039/c3gc37065h
Gamma-valerolactone, a sustainable platform molecule derived from lignocellulosic biomass
resolves10.1016/j.apcatb.2015.04.030
Catalytic reactions of gamma-valerolactone: A platform to fuels and value-added chemicals
resolves10.1002/anie.201307564
Expanding the Scope of Biomass‐Derived Chemicals through Tandem Reactions Based on Oxorhenium‐Catalyzed Deoxydehydration
resolves10.1002/anie.201310991
Highly Efficient Chemical Process To Convert Mucic Acid into Adipic Acid and DFT Studies of the Mechanism of the Rhenium‐Catalyzed Deoxydehydration
resolves10.1002/anie.201102156
Caprolactam from Renewable Resources: Catalytic Conversion of 5‐Hydroxymethylfurfural into Caprolactone
resolves10.1039/b705782b
Towards ‘bio-based’ Nylon: conversion of γ-valerolactone to methyl pentenoate under catalytic distillation conditions
resolves10.1016/S0022-328X(97)00396-3
Highly regioselective hydroformylation of internal, functionalized olefins applying Pt/Sn complexes with large bite angle diphosphines
resolves10.1002/cssc.201301397
Catalytic Conversion of γ‐Valerolactone to ε‐Caprolactam: Towards Nylon from Renewable Feedstock
resolves10.1002/cssc.201200841
Ionic‐Liquid‐Catalyzed Efficient Transformation of γ‐Valerolactone to Methyl 3‐Pentenoate under Mild Conditions
resolves10.1002/9783527619481
Handbook of Metathesis
resolves10.1039/B816917A
Renewable materials as precursors of linear nitrile-acid derivatives viacross-metathesis of fatty esters and acids with acrylonitrile and fumaronitrile
resolves10.1039/b600956e
High conversion and productive catalyst turnovers in cross-metathesis reactions of natural oils with 2-butene
resolves10.1039/C4GC00273C
Olefin cross-metathesis as a valuable tool for the preparation of renewable polyesters and polyamides from unsaturated fatty acid esters and carbamates
resolves10.1039/B604767J
Preparation of terminal oxygenates from renewable natural oils by a one-pot metathesis–isomerisation–methoxycarbonylation–transesterification reaction sequence
resolves10.1016/j.bmcl.2011.01.134
Discovery of histone deacetylase 8 selective inhibitors
resolves10.1016/j.ejmech.2014.01.012
Synthesis and evaluation of new coumarin derivatives as potential atypical antipsychotics
The 1 reference without a DOI — listed, not checked
no DOI — not checkedT. Werpy and G.Petersen, in Top Value Added Chemicals From Biomass Volume I, 2004, vol. 12
What this badge says. CiteStamped means the CHECKABLE references of this work were clean at the dated check: each resolved to a known work in a public registry, and none carried a retraction notice at that time. It says nothing about the quality, findings, or importance of the work itself, and nothing about references deposited without a DOI.

checked 2026-07-22 — re-checked daily as this page is visited; titles and statuses come from Crossref and DataCite and are not part of the signed record

Embed this badge

Both snippets point at the live badge image and link back to this page. The badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.

<a href="https://citestamp.com/citestamped/10.1039/c5gc01922b"><img src="https://citestamp.com/citestamped/10.1039/c5gc01922b/badge.svg" alt="CiteStamped reference-health badge" width="460" height="64"></a>
[![CiteStamped reference-health badge](https://citestamp.com/citestamped/10.1039/c5gc01922b/badge.svg)](https://citestamp.com/citestamped/10.1039/c5gc01922b)