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- Cascade nitrosation and addition–elimination of nitroacetanilides for the highly efficient synthesis of 1,4,2,5-dioxadiazine derivatives. Shanyan Mo, Peipei Huang, Jiaxi Xu
, Org. Biomol. Chem.
, 2014
, 12
, 4192
- Biocatalytic approaches for enantio and diastereoselective synthesis of chiral β-nitroalcohols. D. H. Sreenivasa Rao, Ayon Chatterjee, Santosh Kumar Padhi
, Org. Biomol. Chem.
, 2021
, 19
, 322
- Employment of α-nitroketones in organic synthesis. Chandan Gharui, Subhas chandra Pan
, Org. Biomol. Chem.
, 2019
, 17
, 5190
- Mechanism of nitric acid oxidation of acetophenone to dibenzoylfurazan 2-oxide, benzoic acid, and benzoylformic acid. Hiroshi Tezuka, Megumi Kato, Yukito Sonehara
, J. Chem. Soc., Perkin Trans. 2
, 1985
, 1643
- Convenient synthesis of α-nitrooximes mediated by OXONE®. Napasawan Chumnanvej, Natthapol Samakkanad, Manat Pohmakotr, Vichai Reutrakul, Thaworn Jaipetch, Darunee Soorukram, Chutima Kuhakarn
, RSC Adv.
, 2014
, 4
, 59726
- Organocatalytic asymmetric Michael-type reaction between β,γ-unsaturated α-keto ester and α-nitro ketone. Pengfei Li, Sau Hing Chan, Albert S. C. Chan, Fuk Yee Kwong
, Org. Biomol. Chem.
, 2011
, 9
, 7997
- Does electrophilic activation of nitroalkanes in polyphosphoric acid involve formation of nitrile oxides?. Alexander V. Aksenov, Nicolai A. Aksenov, Nikita K. Kirilov, Anton A. Skomorokhov, Dmitrii A. Aksenov, Igor A. Kurenkov, Elena A. Sorokina, Mezvah A. Nobi, Michael Rubin
, RSC Adv.
, 2021
, 11
, 35937
- Pseudomonas aeruginosa activates the quorum sensing LuxR response regulator through secretion of 2-aminoacetophenone. I. Kviatkovski, L. Chernin, T. Yarnitzky, I. Frumin, N. Sobel, Y. Helman
, Chem. Commun.
, 2015
, 51
, 3258
- Organocatalytic asymmetric Michael/hemiacetalization/acyl transfer reaction of α-nitroketones with o-hydroxycinnamaldehydes: synthesis of 2,4-disubstituted chromans. Rajendra Maity, Subhas Chandra Pan
, Org. Biomol. Chem.
, 2018
, 16
, 1598
- NaI/KI/NH4I and TBHP as powerful oxidation systems: use in the formation of various chemical bonds. Prasanjit Ghosh, Bhaskar Ganguly, Sajal Das
, Org. Biomol. Chem.
, 2021
, 19
, 2146