Some Mechanistic Aspects on Fmoc Solid Phase Peptide Synthesis | SpringerLink
PDF) Oxyma-B, an Excellent Racemization Suppressor in Peptide Synthesis
IJMS | Free Full-Text | Isocyanide Multicomponent Reactions on Solid Phase: State of the Art and Future Application | HTML
![PDF] A comparative study of amide-bond forming reagents in aqueous media – Substrate scope and reagent compatibility | Semantic Scholar](https://ai2-s2-public.s3.amazonaws.com/figures/2017-08-08/5f8253ff990797847606bac48011d4a849802994/4-Figure2-1.png "PDF] A comparative study of amide-bond forming reagents in aqueous media – Substrate scope and reagent compatibility | Semantic Scholar")
PDF] A comparative study of amide-bond forming reagents in aqueous media – Substrate scope and reagent compatibility | Semantic Scholar
Generation of Hydrogen Cyanide from the Reaction of Oxyma (Ethyl Cyano(hydroxyimino)acetate) and DIC (Diisopropylcarbodiimide),Organic Process Research & Development - X-MOL
Minimizing HCN in DIC/Oxyma-Mediated Amide Bond-Forming Reactions,Organic Process Research & Development - X-MOL
Frontiers | Recent Progress in the Chemical Synthesis of Class II and S-Glycosylated Bacteriocins | Microbiology
Figure 10 from Some Mechanistic Aspects on Fmoc Solid Phase Peptide Synthesis | Semantic Scholar
Fmoc Solid Phase Peptide Synthesis of Oxytocin and Analogues | SpringerLink
Coupling Reagents - AAPPTEC
Recent development in peptide coupling reagents - ScienceDirect
PDF) Oxyma-B, an Excellent Racemization Suppressor in Peptide Synthesis
File:DIC HOBt coupling.svg - Wikipedia
Ethyl cyanohydroxyiminoacetate - Wikipedia
Ynamides as Racemization-Free Coupling Reagents for Amide and Peptide Synthesis | Journal of the American Chemical Society
File:Mechanismabcd.png - Wikimedia Commons
Organic Syntheses Procedure
Use of Oxyma as pH modulatory agent to be used in the prevention of base‐driven side reactions and its effect on 2‐chlorotrityl chloride resin - Subirós‐Funosas - 2012 - Peptide Science -
Prevention of aspartimide formation during peptide synthesis using cyanosulfurylides as carboxylic acid-protecting groups | Nature Communications
Oxyma-B, an excellent racemization suppressor for peptide synthesis - Organic & Biomolecular Chemistry (RSC Publishing)
![Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole‐Based HOBt and HOAt with a Lower Risk of Explosion[1] - Subirós‐Funosas - 2009 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/0dbaed69-836e-41f8-8db8-526b3a6e9531/mcontent.jpg "Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole‐Based HOBt and HOAt with a Lower Risk of Explosion[1] - Subirós‐Funosas - 2009 - Chemistry – A European Journal - Wiley Online Library")
Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole‐Based HOBt and HOAt with a Lower Risk of Explosion[1] - Subirós‐Funosas - 2009 - Chemistry – A European Journal - Wiley Online Library
Generation of Hydrogen Cyanide from the Reaction of Oxyma (Ethyl Cyano(hydroxyimino)acetate) and DIC (Diisopropylcarbodiimide) | Organic Process Research & Development
Carbodiimides and Additives - AAPPTEC
基于DIC/Oxyma的蜘蛛毒素多肽GsMTx4的高效合成及活性评价
![Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole‐Based HOBt and HOAt with a Lower Risk of Explosion[1] - Subirós‐Funosas - 2009 - Chemistry – A European Journal - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/f25812e6-46f3-48f3-8b7c-f247189f2dfd/msch002.jpg "Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole‐Based HOBt and HOAt with a Lower Risk of Explosion[1] - Subirós‐Funosas - 2009 - Chemistry – A European Journal - Wiley Online Library")
Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole‐Based HOBt and HOAt with a Lower Risk of Explosion[1] - Subirós‐Funosas - 2009 - Chemistry – A European Journal - Wiley Online Library
