![tert‐Butyl Nitrite (TBN), a Multitasking Reagent in Organic Synthesis - Dahiya - 2019 - Chemistry – An Asian Journal - Wiley Online Library tert‐Butyl Nitrite (TBN), a Multitasking Reagent in Organic Synthesis - Dahiya - 2019 - Chemistry – An Asian Journal - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/465a00fd-d58d-4408-94c4-01307d566f10/asia201901072-fig-5029-m.png)
tert‐Butyl Nitrite (TBN), a Multitasking Reagent in Organic Synthesis - Dahiya - 2019 - Chemistry – An Asian Journal - Wiley Online Library
![tert‐Butyl Nitrite (TBN), a Multitasking Reagent in Organic Synthesis - Dahiya - 2019 - Chemistry – An Asian Journal - Wiley Online Library tert‐Butyl Nitrite (TBN), a Multitasking Reagent in Organic Synthesis - Dahiya - 2019 - Chemistry – An Asian Journal - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/d90dd0ac-ddc4-4f2a-9562-bb204f42ef17/asia201901072-fig-5057-m.png)
tert‐Butyl Nitrite (TBN), a Multitasking Reagent in Organic Synthesis - Dahiya - 2019 - Chemistry – An Asian Journal - Wiley Online Library
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tert -Butyl nitrite-mediated vicinal sulfoximation of alkenes with sulfinic acids: a highly efficient approach toward α-sulfonyl ketoximes - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C6QO00535G
![Mild and efficient TBAI-catalyzed synthesis of 1,2,3-benzotriazine-4-(3H)-ones from tert-butyl nitrite and 2-aminobenzamides under acid-free conditions - ScienceDirect Mild and efficient TBAI-catalyzed synthesis of 1,2,3-benzotriazine-4-(3H)-ones from tert-butyl nitrite and 2-aminobenzamides under acid-free conditions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403916309704-gr1.jpg)
Mild and efficient TBAI-catalyzed synthesis of 1,2,3-benzotriazine-4-(3H)-ones from tert-butyl nitrite and 2-aminobenzamides under acid-free conditions - ScienceDirect
![tert-Butyl nitrite induced radical dimerization of primary thioamides and selenoamides at room temperature - ScienceDirect tert-Butyl nitrite induced radical dimerization of primary thioamides and selenoamides at room temperature - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403917315265-gr3.jpg)
tert-Butyl nitrite induced radical dimerization of primary thioamides and selenoamides at room temperature - ScienceDirect
![tert -Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB01950A tert -Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB01950A](https://pubs.rsc.org/image/article/2018/OB/c8ob01950a/c8ob01950a-s2_hi-res.gif)
tert -Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB01950A
![tert-Butyl nitrite induced radical dimerization of primary thioamides and selenoamides at room temperature - ScienceDirect tert-Butyl nitrite induced radical dimerization of primary thioamides and selenoamides at room temperature - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403917315265-fx1.jpg)
tert-Butyl nitrite induced radical dimerization of primary thioamides and selenoamides at room temperature - ScienceDirect
![Telescopic synthesis of azo compounds via stable arenediazonium bis(trifluoromethane)sulfonimide salts by using tert-butyl nitrite - ScienceDirect Telescopic synthesis of azo compounds via stable arenediazonium bis(trifluoromethane)sulfonimide salts by using tert-butyl nitrite - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0143720816305897-sc2.jpg)
Telescopic synthesis of azo compounds via stable arenediazonium bis(trifluoromethane)sulfonimide salts by using tert-butyl nitrite - ScienceDirect
![tert -Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB01950A tert -Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB01950A](https://pubs.rsc.org/image/article/2018/OB/c8ob01950a/c8ob01950a-s5_hi-res.gif)
tert -Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB01950A
![tert -Butyl nitrite promoted transamidation of secondary amides under metal and catalyst free conditions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB03010C tert -Butyl nitrite promoted transamidation of secondary amides under metal and catalyst free conditions - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C8OB03010C](https://pubs.rsc.org/image/article/2019/OB/c8ob03010c/c8ob03010c-s1_hi-res.gif)