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- Novel approach to biscarbazole alkaloids
via Ullmann coupling – synthesis of murrastifoline-A and bismurrayafoline-A. Carsten Börger, Olga Kataeva, Hans-Joachim Knölker
, Org. Biomol. Chem.
, 2012
, 10
, 7269
- A new route to 1-oxygenated carbazoles. Synthesis of the carbazole alkaloids murrayafoline-A and murrayaquinone-A. Tracey Martin, Christopher J. Moody
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 235
- Iodine-catalyzed aromatization of tetrahydrocarbazoles and its utility in the synthesis of glycozoline and murrayafoline A: a combined experimental and computational investigation. Vivek Humne, Yuvraj Dangat, Kumar Vanka, Pradeep Lokhande
, Org. Biomol. Chem.
, 2014
, 12
, 4832
- First total syntheses of chrestifoline-B and (±)-chrestifoline-C, and improved synthetic routes to bismurrayafoline-A, bismurrayafolinol and chrestifoline-D. Carsten Börger, Arndt W. Schmidt, Hans-Joachim Knölker
, Org. Biomol. Chem.
, 2014
, 12
, 3831
- Palladium-catalyzed cross-dehydrogenative coupling of (hetero)arenes. Gianluigi Albano
, Org. Chem. Front.
, 2024
, 11
, 1495
- Fischer indole synthesis applied to the total synthesis of natural products. Majid M. Heravi, Sahar Rohani, Vahideh Zadsirjan, Nazli Zahedi
, RSC Adv.
, 2017
, 7
, 52852
- Regioselective palladium-catalysed cross-coupling reactions: a powerful synthetic tool. Anant R. Kapdi, Dharmendra Prajapati
, RSC Adv.
, 2014
, 4
, 41245
- A Pd-catalyzed cascade reaction of N–H insertion and oxidative dehydrogenative aromatization: a new entry to 2-amino-phenols. Dong Ding, Xiaobing Lv, Jian Li, Lin Qiu, Guangyang Xu, Jiangtao Sun
, Org. Biomol. Chem.
, 2014
, 12
, 4084
- Cu(i)-catalyzed cross-coupling of primary amines with 2,2′-dibromo-1,1′-biphenyl for the synthesis of polysubstituted carbazole. Yan-Ning Niu, Yan Qiao, Ke-Yu Wang, Bai-Xue Sha, Gao-Qiang Li
, RSC Adv.
, 2022
, 12
, 24232
- Efficient synthesis of biscarbazoles by palladium-catalyzed twofold C–N coupling and C–H activation reactions. Tran Quang Hung, Ngo Ngoc Thang, Do Huy Hoang, Tuan Thanh Dang, Alexander Villinger, Peter Langer
, Org. Biomol. Chem.
, 2014
, 12
, 2596