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- Reactions of 3-bromo-2,3-dihydro- and 2,3-dibromo-4H-1-benzothiopyran-4-one 1,1-dioxides with various amines. Shigeru Watanabe, Hiroyuki Nakazumi, Teijiro Kitao
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 1829
- Ring contractions of thiochroman-4-ones and thiochromen-4-ones. Neil E. MacKenzie, Ronald H. Thomson
, J. Chem. Soc., Perkin Trans. 1
, 1982
, 395
- Synthesis of some thiochromeno[4,3-c]- and [3,4-c]-pyrazoles. Christopher D. Gabbutt, John D. Hepworth, B. Mark Heron, Simon J. Coles, Michael B. Hursthouse
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 2930
- Peculiarities of 2-amino-3-R-4-aryl-4H-pyranes multicomponent synthesis derived from 1H-2,1-benzothiazin-4(3H)-one 2,2-dioxide. Dmitry A. Lega, Nikolay Yu. Gorobets, Valentine P. Chernykh, Svetlana V. Shishkina, Leonid A. Shemchuk
, RSC Adv.
, 2016
, 6
, 16087
- 422. The structure and properties of certain polycyclic indolo- and quinolino-derivatives. Part IV. Derivatives of 1-thiochroman-4-one and of 2-thioisochroman-4-one. A. K. Kiang, Frederick G. Mann
, J. Chem. Soc.
, 1951
, 1909
- Highly efficient construction of spirocyclic chromanone–pyrrolidinesviaCu(i)/TF–BiphamPhos-catalyzed asymmetric 1,3-dipolar cycloaddition. Tang-Lin Liu, Zhao-Lin He, Chun-Jiang Wang
, Chem. Commun.
, 2011
, 47
, 9600
- Non-catalytic approach to the synthesis of partially reduced ‘S’ shaped dioxathia- and oxadithiahelicenes through base induced inter- and intramolecular C–C bond formation. Hardesh K. Maurya, Vishnu K. Tandon, Brijesh Kumar, Abhinav Kumar, Volker Huch, Vishnu Ji Ram
, Org. Biomol. Chem.
, 2012
, 10
, 605
- Partially reduced thiochromene based oxathiahelicenes: crystallographic, computational and Hirschfeld surface analyses. Abhinav Kumar, Volker Hüch, Vishnu Ji Ram
, CrystEngComm
, 2013
, 15
, 7019
- SmI2-mediated reductive cyclization of β-arylthio ketones: a facile and diastereoselective synthesis of thiochroman derivatives. Hui Mao, Bing-Xin You, Lie-Jin Zhou, Ting-Ting Xie, Yi-Hang Wen, Xin Lv, Xiao-Xia Wang
, Org. Biomol. Chem.
, 2017
, 15
, 6157
- Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones. Stuart Aiken, Kelechi Anozie, Orlando D. C. C. de Azevedo, Lewis Cowen, Ross J. L. Edgar, Christopher D. Gabbutt, B. Mark Heron, Philippa A. Lawrence, Abby J. Mills, Craig R. Rice, Mike W. J. Urquhart, Dimitrios Zonidis
, Org. Biomol. Chem.
, 2019
, 17
, 9585