おすすめの製品
アッセイ
≥95%
フォーム
powder
mp
154-159 °C
保管温度
2-8°C
SMILES記法
[N+]3([C@H](CCC3)C(=O)Nc4c(cccc4C(C)C)C(C)C)([O-])CCC[N+]1([C@H](CCC1)C(=O)Nc2c(cccc2C(C)C)C(C)C)[O-]
InChI
1S/C37H56N4O4/c1-24(2)28-14-9-15-29(25(3)4)34(28)38-36(42)32-18-11-20-40(32,44)22-13-23-41(45)21-12-19-33(41)37(43)39-35-30(26(5)6)16-10-17-31(35)27(7)8/h9-10,14-17,24-27,32-33H,11-13,18-23H2,1-8H3,(H,38,42)(H,39,43)/t32-,33-,40?,41?/m1/s1
InChI Key
GRKRBQGUOZNATH-LENWBBSMSA-N
アプリケーション
L3-PrPr2 is a chiral N,N-dioxide ligand developed by the Feng group. In conjunction with a variety of metal salts, this versatile ligand forms and active catalysts complex with application in many different reactions.
関連製品
製品番号
詳細
価格
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
904961-VAR:
904961-BULK:
904961-100MG:
最新バージョンのいずれかを選択してください:
Xin Zhang et al.
The Journal of organic chemistry, 72(14), 5227-5233 (2007-06-15)
Complexes of (S)-pipecolic acid-, L-proline-, and other amino acid-derived N,N'-dioxides coordinated with different metal ions have been investigated in the enantioselective allylation of ketones. A variety of aromatic ketones were found to be suitable substrates in the presence of the
Xiaohu Zhao et al.
Angewandte Chemie (International ed. in English), 54(13), 4032-4035 (2015-02-05)
A highly efficient asymmetric dearomatization of indoles was realized through a cascade reaction between 2-isocyanoethylindole and alkylidene malonates catalyzed by a chiral N,N'-dioxide/Mg(II) catalyst. Fused polycyclic indolines containing three stereocenters were afforded in good yields with excellent diastereo- and enantioselectivities
Hang Zhang et al.
Chemical communications (Cambridge, England), 54(88), 12511-12514 (2018-10-23)
The catalytic asymmetric ene-type reactions of vinylogous hydrazone were accomplished by using chiral N,N'-dioxide-metal salt complexes as catalysts. A wide range of electrophiles, including isatins, α-ketoester, imines, and aldehydes reacted with (E)-2-methyl-N-(piperidin-1-yl)prop-2-en-1-imine efficiently, affording the corresponding homoallylic alcohols and amines
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