Methyl vinyl glycolate as a diverse platform molecule - Green Chemistry (RSC Publishing)
Synthesis, Stability, and Diels‐Alder Reactions of Methyl 2‐Oxobut‐3‐enoate - Jessen - 2021 - European Journal of Organic Chemistry - Wiley Online Library
Methyl vinyl glycolate as a diverse platform molecule - Green Chemistry (RSC Publishing) DOI:10.1039/C6GC01556E
Methyl glycolate 98 96-35-5
5'-DMT-2'-Methyl-A (Bz) Glycolate CPG | LGC, Biosearch Technologies
Methyl vinyl glycolate as a diverse platform molecule - Green Chemistry (RSC Publishing) DOI:10.1039/C6GC01556E
Methyl vinyl glycolate as a diverse platform molecule - Green Chemistry (RSC Publishing) DOI:10.1039/C6GC01556E
Synthesis, Stability, and Diels‐Alder Reactions of Methyl 2‐Oxobut‐3‐enoate - Jessen - 2021 - European Journal of Organic Chemistry - Wiley Online Library
Methyl vinyl ketone (stabilised) for synthesis 78-94-4
/1542E4A41B95DD2A802585F9007982C9/$file/FM32897_structure.png "Methyl glycolate | 96-35-5 | Biosynth Carbosynth")
Methyl glycolate | 96-35-5 | Biosynth Carbosynth
Methyl vinyl glycolate as a diverse platform molecule - Green Chemistry (RSC Publishing)
Molecules | Free Full-Text | A Novel Strategy for Biomass Upgrade: Cascade Approach to the Synthesis of Useful Compounds via C-C Bond Formation Using Biomass-Derived Sugars as Carbon Nucleophiles | HTML
Synthesis, Stability, and Diels‐Alder Reactions of Methyl 2‐Oxobut‐3‐enoate - Jessen - 2021 - European Journal of Organic Chemistry - Wiley Online Library
![Esters_C1-C5 [Non-Heterocyclic Building Blocks] | Tokyo Chemical Industry Co., Ltd.(APAC)](https://www.tcichemicals.com/medias/G0242.jpg?context=bWFzdGVyfHJvb3R8MjYyOTF8aW1hZ2UvanBlZ3xoN2UvaDVjLzg5MzA4MDM3MTIwMzAvRzAyNDIuanBnfDhiODJjNDRjMjVhYzgyY2NiNzMzMDk2NTNlZmI5MmM5NWRlZTY2YTk5ZGIwZjcyOGRiMDVmMTM0MTc0ODJkN2I "Esters_C1-C5 [Non-Heterocyclic Building Blocks] | Tokyo Chemical Industry Co., Ltd.(APAC)")
Esters_C1-C5 [Non-Heterocyclic Building Blocks] | Tokyo Chemical Industry Co., Ltd.(APAC)
Synthesis, Stability, and Diels‐Alder Reactions of Methyl 2‐Oxobut‐3‐enoate - Jessen - 2021 - European Journal of Organic Chemistry - Wiley Online Library
Changing the world of bio-chemicals
Catalytic Transesterification Routes to Novel Vinyl Glycolate Derivatives of Polyhydric Alcohols | SpringerLink
Molecules | Free Full-Text | The Synthesis of Poly(Vinyl Alcohol) Grafted with Fluorinated Protic Ionic Liquids Containing Sulfo Functional Groups
Molecules | Free Full-Text | A Novel Strategy for Biomass Upgrade: Cascade Approach to the Synthesis of Useful Compounds via C-C Bond Formation Using Biomass-Derived Sugars as Carbon Nucleophiles | HTML
Scheme 2 Major pathways, intermediates and products in the conversion... | Download Scientific Diagram
Methyl 2-hydroxybut-3-enoate | C5H8O3 - PubChem
Catalytic Transesterification Routes to Novel Vinyl Glycolate Derivatives of Polyhydric Alcohols | SpringerLink
Methyl vinyl glycolate as a diverse platform molecule - Green Chemistry (RSC Publishing) DOI:10.1039/C6GC01556E
Publications
Tin triflate-catalyzed conversion of cellulose to valuable (α-hydroxy-) esters - ScienceDirect
Methyl vinyl glycolate as a diverse platform molecule - Green Chemistry (RSC Publishing) DOI:10.1039/C6GC01556E
