![Hydrogen Acceptor‐ and Base‐Free N‐Formylation of Nitriles and Amines using Methanol as C1 Source - Kang - 2015 - Advanced Synthesis & Catalysis - Wiley Online Library Hydrogen Acceptor‐ and Base‐Free N‐Formylation of Nitriles and Amines using Methanol as C1 Source - Kang - 2015 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/bba3321a-b5df-45fa-bae2-656e03fea9c5/mcontent.jpg)
Hydrogen Acceptor‐ and Base‐Free N‐Formylation of Nitriles and Amines using Methanol as C1 Source - Kang - 2015 - Advanced Synthesis & Catalysis - Wiley Online Library
![SOLVED: Cyanohydrins are nitrile intermediates in the synthesis of α-hydroxycarboxylic acids from ketones and aldehydes. The Schiobe Tydrokyile fiocica Group can be hydrolyzed by aqueous acid to yield carboxylic acid. Nitriles can SOLVED: Cyanohydrins are nitrile intermediates in the synthesis of α-hydroxycarboxylic acids from ketones and aldehydes. The Schiobe Tydrokyile fiocica Group can be hydrolyzed by aqueous acid to yield carboxylic acid. Nitriles can](https://cdn.numerade.com/ask_images/98c346e0d13c4f6e9126b15703c4c06b.jpg)
SOLVED: Cyanohydrins are nitrile intermediates in the synthesis of α-hydroxycarboxylic acids from ketones and aldehydes. The Schiobe Tydrokyile fiocica Group can be hydrolyzed by aqueous acid to yield carboxylic acid. Nitriles can
![Intramolecular attack on coordinated nitriles: metallacycle intermediates in catalytic hydration and beyond - Dalton Transactions (RSC Publishing) DOI:10.1039/D1DT02795F Intramolecular attack on coordinated nitriles: metallacycle intermediates in catalytic hydration and beyond - Dalton Transactions (RSC Publishing) DOI:10.1039/D1DT02795F](https://pubs.rsc.org/image/article/2021/DT/d1dt02795f/d1dt02795f-s2_hi-res.gif)