Guorong Sheng, Shicong Ma, Songlin Bai, Jing Qian, Kai Huang, Bo Lang, Ping Lu, Yanguang Wang
Index: 10.1016/j.tet.2018.03.021
Full Text: HTML
The rhodium-catalyzed reactions of 3-diazoindolin-2-imines with β-enamino esters furnished 2,3-diaminoindoles in excellent yields with wide functional group tolerance. The synthesized 2,3-diaminoindoles could be converted into 5H-pyrazino [2,3-b]indoles via a sequential dehydrogenation/6π-ERC/aromatization process.
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Synthesis of chiral α-amino anilides via a DMEDA-promoted se...
2018-04-11 [10.1016/j.tet.2018.03.003] |
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A site isolation-enabled organocatalytic approach to enantio...
2018-04-11 [10.1016/j.tet.2018.04.022] |
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Chemoselectivity in the Kosugi-Migita-Stille coupling of bro...
2018-04-10 [10.1016/j.tet.2018.02.051] |
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Process design methodology for organometallic chemistry in c...
2018-04-07 [10.1016/j.tet.2018.04.020] |
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Substrate engineering: Effects of different N-protecting gro...
2018-04-07 [10.1016/j.tet.2018.04.012] |
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