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化驗
99%
形狀
solid
光學活性
[α]21/D +34°, c = 1 in THF
光學純度
ee: 99% (HPLC)
mp
208-210 °C (lit.)
SMILES 字串
Oc1ccc2ccccc2c1-c3c(O)ccc4ccccc34
InChI
1S/C20H14O2/c21-17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)22/h1-12,21-22H
InChI 密鑰
PPTXVXKCQZKFBN-UHFFFAOYSA-N
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應用
一种手性助剂，用于硫化物催化不对称氧化成亚砜。联萘酚生成的手性镧系元素三氟酸盐可作为不对称 Diels-Alder 反应的催化剂。联萘酚的衍生物最近被发现用于不对称 Claisen 重排和不对称环氧化反应。这些二醇的氢化铝锂衍生物 (BINAP-H) 已广泛用于还原酮。
手性联萘酚亚胺鎓盐前体。此盐用于烯烃的不对称环氧化反应。
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2
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, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Asymmetric Diels-Alder reactions catalyzed by chiral lanthanide (III) trifluoromethanesulfonates. Unique structure of the triflate and stereoselective synthesis of both enantiomers using a single chiral source and a choice of achiral ligands.
S. Kobayashi et al.
Tetrahedron, 50(40), 11623-11623 (1994)
New chiral binaphthalene-derived iminium salt organocatalysts for asymmetric epoxidation of alkenes.
Philip C Bulman Page et al.
The Journal of organic chemistry, 72(12), 4424-4430 (2007-05-18)
A series of binaphthalene-fused azepinium salts has been generated and used as organocatalysts in the asymmetric epoxidation of unfunctionalized alkenes, giving rise to ees of up to 84%.
Asymmetric aza-Diels-Alder reaction catalyzed by boron reagent: Effect of biphenol and binaphthol ligand.
Hattori, K. Yamamoto, H.
Synlett, 1993(02), 129-129 (1993)
Catalytic asymmetric oxidation of sulfides to sulfoxides with tert-butyl hydroperoxide using binaphthol as a chiral auxiliary.
Komatsu N, et al.
The Journal of Organic Chemistry, 58, 4529-4529 (1993)
Catalytic asymmetric epoxidation with (Salen) manganese (III) complex bearing binaphthyl groups of axial chirality.
Sasaki, H. et al.
Synlett, 1993(04), 300-300 (1993)
商品
我们展示了一篇有关BINOL及其衍生物的文章。
We present an article concerning BINOL and Derivatives.
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