Abstract
Structure/activity relations in chiral drugs can only be studied if the absolute configuration is known. The levorotatory form of the cancerostatic isophos‐phamide is shown by X‐ray structure analysis to have the S configuration.
Original language | English (US) |
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Pages (from-to) | 549-550 |
Number of pages | 2 |
Journal | Angewandte Chemie International Edition in English |
Volume | 19 |
Issue number | 7 |
DOIs | |
State | Published - Jul 1980 |
Externally published | Yes |