4-81-75
| 规格 | 目录价格 | 上海 | 安徽 | 武汉 | 成都 | 北方 | 深圳 | 会员价格 | 数量 |
|---|---|---|---|---|---|---|---|---|---|
| 1g | ￥ ȋǕÿǕǕ | 1 | > 1 | -- | -- | -- | -- | ￥ ȋǕÿǕǕ | - + |
| 5g | ￥ ēǕÿǕǕ | -- | > 1 | -- | -- | -- | -- | ￥ ēǕÿǕǕ | - + |
| 1g | ￥ NJŮŮÿǕǕ | -- | > 1 | -- | -- | -- | -- | ￥ NJŮŮÿǕǕ | - + |
| 5g | ￥ ƨNJēNJÿǕǕ | -- | > 1 | -- | -- | -- | -- | ￥ ƨNJēNJÿǕǕ | - + |
| 1kg | ￥ NJŮȋƨÿǕǕ | -- | > 1 | -- | -- | -- | -- | ￥ NJŮȋƨÿǕǕ | - + |
| 大货 | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
4.46
[1]. Ben W Glasspoole, et al. Suzuki-Miyaura cross-couplings of secondary allylic boronic esters. Chem Commun (Camb). 1 Jan 3;48(9):13-.
[]. Dietrich Steinhuebel, et al. Enol tosylates as viable partners in Pd-catalyzed cross-coupling reactions. J Org Chem. 5 Nov 5;7(4):114-7.
[3]. Hui-Xiong Dai, et al. Divergent C-H functionalizations directed by sulfonamide pharmacophores: late-stage diversification as a tool for drug discovery. J Am Chem Soc. 11 May 11;133(18):7-8.
[4]. Ling Zhou, et al. Asymmetric bromolactonization using amino-thiocarbamate catalyst. J Am Chem Soc. 1 Nov 1;13(44):15474-6.
[5]. Ling Zhou, et al. Enantioselective bromoaminocyclization using amino-thiocarbamate catalysts. J Am Chem Soc. 11 Jun ;133(4):9164-7.
P61-P64-P71-P8-P3+P35-P34+P34-P36+P364-P45-P51
GHS7
13776 现货
￥ ȋȋÿǕǕ -5g
171 货期咨询
￥ ŽȋĊÿǕǕ -1g
14756 货期咨询
￥ ȋƢǕǕÿǕǕ -1g
1937658 货期咨询
18441 货期咨询
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