108832-95-7Relevant articles and documents
An efficient synthesis of both enantiomers of Cathinone by regioselective reductive ring opening of substituted aziridines
Hwang, Gweon Il,Chung, Jae-Ho,Lee, Won Koo
, p. 12111 - 12116 (1996)
Both enantiomers of Cathinone were prepared as HCl salts from N-(R)-α-methylbenzylaziridine-2(S)-carboxaldehyde 2c and its enantiomer N-(S)-α-methyl-benzylaziridine-2(R)-carboxaldehyde 3c in high yield. This process makes it possible to prepare other aromatic and heteroaromatic analogs of Cathinone efficiently.
Conjugates of Cell Binding Molecules with Cytotoxic Agents
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, (2017/11/06)
A conjugate of a potent cytotoxic agent with a cell-surface receptor binding molecule having a Formula (I), wherein T, L, m, n, R1, R2, R3, R4, R5, R6, R7, R8, R9
CONJUGATES OF CELL BINDING MOLECULES WITH CYTOTOXIC AGENTS
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, (2017/07/15)
A conjugate of a potent cytotoxic agent with a cell-surface receptor binding molecule having a formula (I), wherein T, L, m, n, Y, R1, R2, R3, R4, R5, R6, R7, R8, Rsu