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Merck
CN

675156

(R)-VANOL

97%

别名:

(2R)-(+)-3,3′-二苯基-[2,2′-联二萘]-1,1′-二醇, (R)-3,3′-二苯基-2,2′-二-1-萘酚

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关于此项目

经验公式（希尔记法）:
C32H22O2
化学文摘社编号:
147702-13-4
分子量:
438.52
MDL编号:
MFCD08459338
UNSPSC代码:
12352005
PubChem化学物质编号:
24885264
NACRES:
NA.22

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方案

97%

表单

solid

旋光性

[α]20/D +310°, c = 1 in chloroform

mp

200-204 °C

官能团

phenyl

SMILES字符串

Oc1c(c(cc2ccccc12)-c3ccccc3)-c4c(O)c5ccccc5cc4-c6ccccc6

InChI

1S/C32H22O2/c33-31-25-17-9-7-15-23(25)19-27(21-11-3-1-4-12-21)29(31)30-28(22-13-5-2-6-14-22)20-24-16-8-10-18-26(24)32(30)34/h1-20,33-34H

InChI key

NDTDVKKGYBULHF-UHFFFAOYSA-N

相关类别

应用

已证实 VANOL 是用于催化型不对称 Diels-Alder 反应、亚胺羟醛反应以及氮杂环丙化反应的绝佳配体。
(R)-VANOL is a vaulted biaryl ligand that may be used in the following processes:
  • Transformation of 3-substituted cyclobutanones to enantiopure γ-butyrolactones via asymmetric Baeyer-Villiger Reaction in the presence of an aluminum catalyst.
  • Asymmetric aziridination of N-(4-(Methylsulfonyl)benzylidene)diphenylmethanamine to form (2S,3S)-ethyl 1-benzhydryl-3-(4-(methylsulfonyl)phenyl) aziridine-2-carboxylate.
  • Conjugate addition of terminal alkynes to 2-arylidene-1,3-diketones with high enantioselectivity in the presence of diethyl zinc.

象形图

CorrosionExclamation mark
GHS05,GHS07

警示用语：

Danger

危险分类

Aquatic Chronic 4 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKBW4021V
MKBJ6613V
06428DJ
13305HE

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Vaulted biaryls: efficient ligands for the aluminum-catalyzed asymmetric Baeyer-Villiger reaction.
Bolm C, et al.
Synlett, 2004(09), 1619-1621 (2004)
Blay G, et al.
Chemistry?A European Journal , 18(41), 12966-12969 (2012)
An efficient enantioselective synthesis of florfenicol via asymmetric aziridination.
Wang Z, et al.
Tetrahedron, 67(47), 9199-9203 (2011)
Su Yu et al.
Organic letters, 7(3), 367-369 (2005-01-28)
[reaction: see text] In an effort to develop a synthesis of the VAPOL ligand that avoids the use of a chromium carbene complex, a route was examined that involved the annulation of a naphthalene carboxamide via the method of Snieckus.
Bao. J. et al.
Journal of the American Chemical Society, 118, 3392-3392 (1996)
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