规格 | 目录价格 | 上海 | 安徽 | 武汉 | 成都 | 北方 | 深圳 | 会员价格 | 数量 |
---|---|---|---|---|---|---|---|---|---|
g | ¥ ƩȢĽIJƵƵ | -- | -- | -- | -- | -- | -- | ¥ ƩȢĽIJƵƵ | - + |
5g | ¥ ŷƵŷIJƵƵ | -- | -- | -- | -- | -- | -- | ¥ ŷƵŷIJƵƵ | - + |
g | ¥ džŋȍĽIJƵƵ | -- | -- | -- | -- | -- | -- | ¥ džŋȍĽIJƵƵ | - + |
5g | ¥ ƩȢĽŷIJƵƵ | -- | -- | -- | -- | -- | -- | ¥ ƩȢĽŷIJƵƵ | - + |
g | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
5g | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
g | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
.3
[]. A Olma, et al. A convenient route to optically pure α-alkyl-β-(sec-amino)alanines. Amino Acids. Jun;4(6):55-8.
[]. B Beck, et al. One-pot multicomponent synthesis of two novel thiolactone scaffolds. Mol Divers. Aug;4(3):479-9.
[3]. B Combourieu, et al. Common degradative pathways of morpholine, thiomorpholine, and piperidine by Mycobacterium aurum MO: evidence from ()H-nuclear magnetic resonance and ionspray mass spectrometry performed directly on the incubation medium. Appl Environ Microbiol. Aug;66(8):387-93.
[4]. Cam-Van T Vo, et al. SnAP reagents for the transformation of aldehydes into substituted thiomorpholines--an alternative to cross-coupling with saturated heterocycles. Angew Chem Int Ed Engl. 3 Feb 4;5(6):75-8.
[5]. Claire L Jarvis, et al. Redox-neutral α-sulfenylation of secondary amines: ring-fused N,S-acetals. Org Lett. 4 Jul 3;6(3):3556-9.
P6-P64-P7-P7-P8-P3+P35-P34+P34-P35+P35+P338-P33-P36+P364-P43+P33-P45-P5