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AJE 润色服务限时 8 折起，权威机构信任 15+ 年Cytoscape 教程来了！快速实现顶刊同款通路网络图五大应用案例：Mustang Q 膜层析应用全解析1 个小工具，一次性搞定流程图、质粒图谱和信号通路图- 详细信息
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- 英文名：
tert-Butyl (Z)-(4-Bromo-3-fluorobut-2-en-1yl)carbamate
- 库存：
100+
- 供应商：
上海维亦特生物
- CAS号：
1098972-51-0
tert-Butyl (Z)-(4-Bromo-3-fluorobut-2-en-1yl)carbamate
1098972-51-0
C₉H₁₅BrFNO₂
268.12
No Data Available
No Data Available
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文献和实验tert-Butyl (Z)-(4-Bromo-3-fluorobut-2-en-1yl)carbamate
1098972-51-0
C₉H₁₅BrFNO₂
268.12
No Data Available
No Data Available
Natural Product Chemistry in Action: The Synthesis of Melatonin Metabolites K1 and K2
melatonin, the kynurenamines N1-acetyl-N2 -formyl-5-methoxykynurenine (K1 ) and N -acetyl-5-methoxykynurenamine (K2 ). The four key synthetic transformations involve (a) conversion of 4-methoxy aniline into the tert -butyl (4-methoxyphenyl)carbamate, (b
Synthesis of Peptidomimetic Conjugates of Cyclic Nucleoside Phosphonates
to 200 mesh, 1% cross‐linked, typical loading 1.0 to 1.8 mmol/g; Aldrich) Methyl O‐[tert‐butyl(dimethyl)silyl]‐(L )‐serinate ( S.6 a , see protocol
Uridine 2′‐Carbamates: Facile Tools for Oligonucleotide 2′‐Functionalization
for preparation of uridine 2??carbamate derivatives based on reaction of 3?,5??disilyl?protected uridine with 1,1??carbonyldiimidazole followed by treatment with an aliphatic amine is presented. A phosphoramidite monomer suitable for automated oligonucleotide
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