The stereoselectivities of tributyltin hydride-mediated reductions of 5-bromo-D-glucuronides to L-iduronides are dependent on the anomeric substituent: syntheses and DFT calculations.
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The stereoselectivities of tributyltin hydride-mediated reductions of 5-bromo-D-glucuronides to L-iduronides are dependent on the anomeric substituent: syntheses and DFT calculations.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
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2016年學術文章
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2016年學術文章
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name
The stereoselectivities of tri ...... yntheses and DFT calculations.
@en
The stereoselectivities of tri ...... yntheses and DFT calculations.
@nl
type
label
The stereoselectivities of tri ...... yntheses and DFT calculations.
@en
The stereoselectivities of tri ...... yntheses and DFT calculations.
@nl
prefLabel
The stereoselectivities of tri ...... yntheses and DFT calculations.
@en
The stereoselectivities of tri ...... yntheses and DFT calculations.
@nl
P2860
P356
P1476
The stereoselectivities of tri ...... yntheses and DFT calculations.
@en
P2093
Shifaza Mohamed
Vito Ferro
P2860
P304
P356
10.1039/C6OB00283H
P577
2016-03-01T00:00:00Z