![PDF] tert-Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature. | Semantic Scholar PDF] tert-Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/1ccc8dbf3ffb4ace8b7cc02a374671c6d75a1021/2-Figure1-1.png)
PDF] tert-Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature. | Semantic Scholar
![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 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](https://pubs.rsc.org/image/article/2017/QO/c6qo00535g/c6qo00535g-s3_hi-res.gif)
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
![Tert-butyl nitrite : a metal-free radical initiator for aerobic cleavage of benzylic C[double bond, length as m-dash]C bonds in compressed carbon dio ... - Green Chemistry (RSC Publishing) DOI:10.1039/C0GC00676A Tert-butyl nitrite : a metal-free radical initiator for aerobic cleavage of benzylic C[double bond, length as m-dash]C bonds in compressed carbon dio ... - Green Chemistry (RSC Publishing) DOI:10.1039/C0GC00676A](https://pubs.rsc.org/image/article/2011/GC/c0gc00676a/c0gc00676a-s3.gif)
Tert-butyl nitrite : a metal-free radical initiator for aerobic cleavage of benzylic C[double bond, length as m-dash]C bonds in compressed carbon dio ... - Green Chemistry (RSC Publishing) DOI:10.1039/C0GC00676A
![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 (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/253dfbdf-5fa1-4b6b-889f-faaff5520537/asia201901072-fig-5028-m.png)
tert‐Butyl Nitrite (TBN), a Multitasking Reagent in Organic Synthesis - Dahiya - 2019 - Chemistry – An Asian Journal - Wiley Online Library
![tert‐Butyl Nitrite Mediated Different Functionalizations of Internal Alkenes: Paths to Furoxans and Nitroalkenes - Mir - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library tert‐Butyl Nitrite Mediated Different Functionalizations of Internal Alkenes: Paths to Furoxans and Nitroalkenes - Mir - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/fbb6d0d2-9d40-4889-99a0-cded98479198/adsc201800668-toc-0001-m.jpg)
tert‐Butyl Nitrite Mediated Different Functionalizations of Internal Alkenes: Paths to Furoxans and Nitroalkenes - Mir - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library
![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 (TBN) as the N atom source for the synthesis of substituted cinnolines with 2-vinylanilines and a relevant mechanism was studied ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C7OB01553D tert -Butyl nitrite (TBN) as the N atom source for the synthesis of substituted cinnolines with 2-vinylanilines and a relevant mechanism was studied ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C7OB01553D](https://pubs.rsc.org/image/article/2017/OB/c7ob01553d/c7ob01553d-s1_hi-res.gif)
tert -Butyl nitrite (TBN) as the N atom source for the synthesis of substituted cinnolines with 2-vinylanilines and a relevant mechanism was studied ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C7OB01553D
![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 (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/46460585-00d9-4495-a6b4-f409277f94d0/asia201901072-fig-5060-m.png)
tert‐Butyl Nitrite (TBN), a Multitasking Reagent in Organic Synthesis - Dahiya - 2019 - Chemistry – An Asian Journal - Wiley Online Library
![Table 3 from tert-Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature. | Semantic Scholar Table 3 from tert-Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/1ccc8dbf3ffb4ace8b7cc02a374671c6d75a1021/5-Table3-1.png)
Table 3 from tert-Butyl nitrite mediated nitrogen transfer reactions: synthesis of benzotriazoles and azides at room temperature. | Semantic Scholar
![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)
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 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
tert-Butyl nitrite (TBN) as the N atom source for the synthesis of substituted cinnolines with 2-vinylanilines and a relevant mechanism was studied - Organic & Biomolecular Chemistry (RSC Publishing)
![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/276a20a1-69a3-4804-a091-739e48622d39/asia201901072-fig-5070-m.png)