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- Electrochemical reactions. Part II. The structure of an unusual product from the reduction of 1-acetylnaphthalene. J. Grimshaw, E. J. F. Rea
, J. Chem. Soc. C
, 1967
, 2628
- 4-Amino-2,3,4,5-tetrahydro-1-benzoxepin-5-ols, 4-amino-2,3,4,5-tetrahydro-1-benzothiepin-5-ols, and related compounds. D. Huckle, I. M. Lockhart, N. E. Webb
, J. Chem. Soc. C
, 1971
, 2252
- 4,5-Dihydro-1-benzoxepin-3(2H)-one, N-substituted 2,3-dihydro-1,5-benzoxazepin-4(5H)-ones, and related compounds. D. Huckle, I. M. Lockhart, M. Wright
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 2425
- Dimeric and trimeric flavonoids containing a cyclopentane ring: 6,7-diaryl-6a,7,13,13a-tetrahydro-6H-7,13-methano[1]benzopyrano[3,4-c][1]benzoxepins. Ben R. Brown, A. William R. Tyrrell
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 1963
- The alkylation and ring-expansion of chromones by diazoalkanes; reluctance of oxygen to engage in sigmatropic shifts. Francis M. Dean, Robert S. Johnson
, J. Chem. Soc., Perkin Trans. 1
, 1981
, 224
- Reaction of 1-benzoxepin with singlet oxygen: a novel endoperoxide. Jack E. Baldwin, O. William Lever
, J. Chem. Soc., Chem. Commun.
, 1973
, 344
- 3,7-Bis(hydroxymethyl)-1-benzoxepin-5(2H)-one, a novel oxygen heterocyclic metabolite from cultures of the fungus Marasmiellus ramealis(Bull. ex Fr.) singer. John K. Holroyde, Alex F. Orr, Viktor Thaller
, J. Chem. Soc., Perkin Trans. 1
, 1978
, 1490
- Controlling the selectivity of an intramolecular Friedel–Crafts alkylation with alkenes using selenium under mild conditions. Ming-Hong Liao, Meng Zhang, Dai-Hui Hu, Rui-Han Zhang, Yan Zhao, Shan-Shan Liu, Yun-Xia Li, Wei-Lie Xiao, E Tang
, Org. Biomol. Chem.
, 2020
, 18
, 4034
- Rearrangement of dithianylcyclobutachromanol derivatives to 1,2,2a,8,9,9a-hexahydrocyclobuta[b][1]benzoxepin-8,9-dione. Brindaban C. Ranu, Sanjay Bhar, Amarendra Patra, Nirmalya P. Nayak, Monika Mukherjee
, Chem. Commun.
, 1996
, 1965
- Recent progress in selective estrogen receptor downregulators (SERDs) for the treatment of breast cancer. Shagufta, Irshad Ahmad, Shimy Mathew, Sofia Rahman
, RSC Med. Chem.
, 2020
, 11
, 438