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Merck

794287

Sigma-Aldrich

Bis[(pinacolato)boryl]methane

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别名:

2,2′-Methylenebis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane], Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methane

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About This Item

经验公式(希尔记法):
C13H26B2O4
CAS号:
分子量:
267.97
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.22

形狀

solid

品質等級

環保替代產品特色

Catalysis
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sustainability

Greener Alternative Product

mp

48 °C

環保替代類別

儲存溫度

2-8°C

SMILES 字串

CC(C(C)(C)O1)(C)OB1CB2OC(C)(C)C(C)(C)O2

InChI

1S/C13H26B2O4/c1-10(2)11(3,4)17-14(16-10)9-15-18-12(5,6)13(7,8)19-15/h9H2,1-8H3

InChI 密鑰

MQYZGGWWHUGYDR-UHFFFAOYSA-N

一般說明

Bis[(pinacolato)boryl]methane is an aryl boronate ester.
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應用

Bis-boronate has been reported by Morken and coworkers to be a key building block in the synthesis of enantioenriched secondary boronate esters, which undergo facile Suzuki-Miyaura coupling with minimal erosion of enantiopurity.
Bis[(pinacolato)boryl]methane may be used in the preparation of trans-vinyl boronate esters, via the Boron-Wittig reaction.

象形圖

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訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3


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John R Coombs et al.
Organic letters, 17(7), 1708-1711 (2015-03-24)
A highly stereoselective boron-Wittig reaction between stable and readily accessible 1,1-bis(pinacolboronates) and aldehydes furnishes a variety of synthetically useful di- and trisubstituted vinyl boronate esters.
A Catalytic Enantiotopic-Group-Selective Suzuki Reaction for the Construction of Chiral Organoboronates
Sun C, et al.
Journal of the American Chemical Society, 136, 6534-6537 (2014)

相关内容

Enantioselective alkene diboration is a valuable strategy for transforming unsaturated hydrocarbons into useful chiral building blocks.

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