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Scheme 1

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ZDB-IMAGE-240503-54
Source
Figures for Ma et al., 2024
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Figure Caption

Scheme 1 (A) Synthesis of clickable version of DEAC450 3. (B) Synthesis of DEAC450 caged ATP 6. (a) ETT, DMF, r.t., 5 min. (b) mCPBA, DMF, 0 °C, 5 min. (c) 5–10% (v/v) piperidine, r.t., 40 min, in DMF. The product is obtained as triethylammonium (TEA) salt after purification. (C) Synthesis of dendronized DEAC450 caged ATPs with different transporters attached and structures of dendrons used in this study.

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