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Merck
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文件

526304

Sigma-Aldrich

聚合物负载氰基硼氢化物

macroporous, 20-50 mesh, extent of labeling: ~2.0-3.5 mmol/g loading

同義詞:

Amberlite™ IRA-400 负载氰基硼氢化物

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About This Item

分類程式碼代碼:
12352117
PubChem物質ID:
329757864
NACRES:
NA.22

形狀

macroporous

反應適用性

reaction type: solution phase peptide synthesis
reactivity: imine reactive

標籤範圍

~2.0-3.5 mmol/g loading

粒徑

20-50 mesh

mp

>300 °C (lit.)

儲存溫度

2-8°C

一般說明

Cyanoborohydride, polymer supported: is a polymer-supported reducing agent used in reductive amination reactions at room temperature.

應用

Polymer supported cyanoborohydride (PSCBH) has been used in the reductive alkylation aminocyclitols for the preparation of corresponding secondary amines.
It can also be used:
  • In combination with manganese dioxide (MnO2) for one-pot conversion of alcohols to secondary or tertiary amines.
  • In the synthesis of natural products, (±)-oxomaritidine and (±)-epimaritidine.

法律資訊

Amberlite is a trademark of DuPont de Nemours, Inc.

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

分析證明 (COA)

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Ley, S.V.
J. Chem. Soc., Perkin Trans., 2239-2239 (1998)
In situ oxidation- imine formation- reduction routes from alcohols to amines
Blackburn L and Taylor RJK
Organic Letters, 3(11), 1637-1639 (2001)
Small-Scale One-Pot Reductive Alkylation of Unprotected Aminocyclitols with Supported Reagents
Sisa M, et al.
Synthesis, 2008(19), 3167-3170 (2008)
Hutchins, R.O. et al.
Journal of the Chemical Society. Chemical Communications, 1088-1088 (1978)
Synthesis of the alkaloids (?)-oxomaritidine and (?)-epimaritidine using an orchestrated multi-step sequence of polymer supported reagents
Ley S, et al.
Journal of the Chemical Society. Perkin Transactions 1, 3(10), 1251-1252 (1999)
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