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- Room-temperature crystallography using a microfluidic protein crystal array device and its application to protein–ligand complex structure analysis. Masatoshi Maeki, Sho Ito, Reo Takeda, Go Ueno, Akihiko Ishida, Hirofumi Tani, Masaki Yamamoto, Manabu Tokeshi
, Chem. Sci.
, 2020
, 11
, 9072
- Directed evolution of RebH for catalyst-controlled halogenation of indole C–H bonds. Mary C. Andorfer, Hyun June Park, Jaylie Vergara-Coll, Jared C. Lewis
, Chem. Sci.
, 2016
, 7
, 3720
- Electrochemical bromocyclization enables 3,5-diversification of heterocyclic indolines. Hai Ren, Rui-An Wang, Jun Shi, Jun-Rong Song, Wei Wu, Qin Chi, Ni Zhang
, Org. Biomol. Chem.
, 2023
, 21
, 7290
- Catalytic asymmetric preparation of pyrroloindolines: strategies and applications to total synthesis. Guang-Jian Mei, Wai Lean Koay, Chuan Xiang Alvin Tan, Yixin Lu
, Chem. Soc. Rev.
, 2021
, 50
, 5985
- Reactions of tryptophols and N
α-acetyltryptamines with iodine azide. Formation of 3a-azido-3,3a,8,8a-tetrahydro-2H-furo- and 3a-azido-1,2,3,3a,8,8a-hexahydropyrrolo-[2,3-b]indoles. Masazumi Ikeda, Kazunori Ohno, Misuzu Katsura, Moon-Woo Chun, Yasumitsu Tamura
, J. Chem. Soc., Perkin Trans. 1
, 1979
, 3061
- Titanium catalysis for the synthesis of fine chemicals – development and trends. Manfred Manßen, Laurel L. Schafer
, Chem. Soc. Rev.
, 2020
, 49
, 6947
- 1058. The protonation of tryptamine derivatives in acidic media. A. H. Jackson, A. E. Smith
, J. Chem. Soc.
, 1964
, 5510
- Indolization by phosphorus trichloride of functionalized ketone arylhydrazones: synthesis of pharmacological interesting indoles. Grazieno Baccolini, Renato Dalpozzo, Paolo E. Todesco
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 971
- A synthesis of 2-alkyltryptamines and of 3,4-dihydro-β-carboline. Ian Fleming, John Harley-Mason
, J. Chem. Soc. C
, 1966
, 425
- Physiologically active compounds interacting with serotonin (5-hydroxytryptamine) receptors. Ol'ga N. Zefirova, Nikolai S. Zefirov
, Russ. Chem. Rev.
, 2001
, 70
, 333