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- A new strategy for the synthesis of pyridines from N-propargylic β-enaminothiones. Yilmaz Kelgokmen, Metin Zora
, Org. Biomol. Chem.
, 2019
, 17
, 2529
- A sequential synthetic strategy towards unexplored dibenzo[b,f][1,4]thiazepine carboxamides: copper catalysed C–S cyclisation followed by Ugi type 3CC cascade. Debasmita Saha, Preeti Wadhwa, Anuj Sharma
, RSC Adv.
, 2015
, 5
, 33067
- A transition metal-free tandem process to pyridazinopyrido[3,2-f][1,4]thiazepine-diones via Smiles rearrangement. Xiaoyi Niu, Bingchuan Yang, Yanqiu Li, Shuai Fang, Zixiao Huang, Caixia Xie, Chen Ma
, Org. Biomol. Chem.
, 2013
, 11
, 4102
- Benzothiazepines: chemistry of a privileged scaffold. Debasmita Saha, Garima Jain, Anuj Sharma
, RSC Adv.
, 2015
, 5
, 70619
- Ultrasound promoted catalyst-free and selective synthesis of spiro[indole-3,4′-pyrazolo[3,4-e][1,4]thiazepines] in aqueous media and evaluation of their anti-hyperglycemic activity. Anshu Dandia, Ruby Singh, Jyoti Joshi, Shuchi Maheshwari, Pragya Soni
, RSC Adv.
, 2013
, 3
, 18992
- Asymmetric hydrogenation of dibenzo-fused azepines with chiral cationic ruthenium diamine catalysts. Zi-Qi Yi, Bo-Wen Deng, Fei Chen, Yan-Mei He, Qing-Hua Fan
, New J. Chem.
, 2023
, 47
, 11492
- Reduction of nitro- and nitroso-compounds by tervalent phosphorus reagents. Part IX. The ‘blocked ortho’ effect in reactions of 2,6-di-substituted aryl 2-nitrophenyl and 2,6-disubstituted aryl 2-azidophenyl sulphides: a new series of nitrene-induced aromatic rearrangements. J. I. G. Cadogan, S. Kulik
, J. Chem. Soc. C
, 1971
, 2621
- A new aromatic rearrangement involving a nitrene: synthesis of the 5,11-dihydrodibenzo[b,e]-1,4-thiazepine ring system. J. I. G. Cadogan, S. Kulik
, J. Chem. Soc. D
, 1970
, 233
- The new synthesis of pyrrole-fused dibenzo[b,f][1,4]oxazepine/thiazepines by the pseudo-Joullié–Ugi reaction via an unexpected route with high chemoselectivity. Mohammad Taghi Nazeri, Masoomeh Ahmadi, Maryam Ghasemi, Ahmad Shaabani, Behrouz Notash
, Org. Biomol. Chem.
, 2023
, 21
, 4095
- Studies related to penicillins. Part IV. The rearrangement of penicillanic acid derivatives to 1,4-thiazepines. J. P. Clayton, R. Southgate, B. G. Ramsay, R. J. Stoodley
, J. Chem. Soc. C
, 1970
, 2089