Chemical Communications

Journal Information
ISSN / EISSN : 1359-7345 / 1364-548X
Current Publisher: Royal Society of Chemistry (RSC) (10.1039)
Total articles ≅ 60,804
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Latest articles in this journal

Yuki Kodama, Saki Imai, Junko Fujimoto, Kohei Sato, Nobuyuki Mase, Tetsuo Narumi
Chemical Communications; doi:10.1039/d1cc02952e

The publisher has not yet granted permission to display this abstract.
Saeed Saeed, Shelby Boyd, Wan-Yu Tsai, Ruocun Wang, Nina Balke, Veronica Augustyn
Chemical Communications; doi:10.1039/d1cc01681d

The publisher has not yet granted permission to display this abstract.
Tal Ben Uliel, Eliyahu M. Farber, Hagit Aviv, Wowa Stroek, Marilena Ferbinteanu, Yaakov R. Tischler, David Eisenberg
Chemical Communications; doi:10.1039/d1cc00420d

The publisher has not yet granted permission to display this abstract.
, Constantinos G. Neochoritis, Xiaofang Lei, Panagiota Lampiri, Giasemi K. Angeli, Pravin Patil
Chemical Communications; doi:10.1039/d1cc02384e

Abstract:
The ubiquitous presence of the indole fragment in natural products and drugs asks forever novel syntheses. We report an unprecedented mild, two-step synthesis of 2-tetrazolo substituted indoles based on the...
Qi Ding, Chen Li, Haijun Wang, Chuanlai Xu, Hua Kuang
Chemical Communications; doi:10.1039/d1cc00983d

The publisher has not yet granted permission to display this abstract.
Xiaohan Wang, Riku Enomoto,
Chemical Communications; doi:10.1039/d1cc01857d

The publisher has not yet granted permission to display this abstract.
Mengsi Zhang, Meiyan Cui, Zhiying Zhao, Xing Huang, Zhangzhen He
Chemical Communications; doi:10.1039/d1cc02243a

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Yasunori Toda, Minoru Shishido, Tatsuya Aoki, Kimiya Sukegawa, Hiroyuki Suga
Chemical Communications; doi:10.1039/d1cc02493k

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Tomoki Hirohata, Naoki Shida, Hidehiro Uekusa, Nobuhiro Yasuda, , Tomoki Ogoshi, ,
Chemical Communications; doi:10.1039/d1cc02413b

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Katarina Stefkova, Matthew J. Heard, ,
Chemical Communications; doi:10.1039/d1cc01856f

Abstract:
Triarylboranes have gained substantial attention as catalysts for C–C bond forming reactions due to their remarkable catalytic activities. Herein, we report B(C6F5)3 catalysed cyclopropenation of a wide variety of arylacetylenes using donor–acceptor diazoesters. A mild reaction protocol has been developed for the synthesis of functionalised cyclopropenes (33 examples) in good to excellent yields.
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