Fmoc-L-Tyr(tBu)-ol
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Fmoc-L-Tyr(tBu)-ol

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Category
Amino Alcohol
Catalog number
BAT-000635
CAS number
187526-99-4
Molecular Formula
C28H31NO4
Molecular Weight
445.5
Fmoc-L-Tyr(tBu)-ol
IUPAC Name
9H-fluoren-9-ylmethyl N-[(2S)-1-hydroxy-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propan-2-yl]carbamate
Synonyms
Fmoc-L-Tyrosinol(tBu); Fmoc-O-tert-butyl-L-tyrosinol
Appearance
White powder
Purity
≥ 98% (HPLC)
Melting Point
~ 120 ºC
Storage
Store at 2-8 °C
InChI
InChI=1S/C28H31NO4/c1-28(2,3)33-21-14-12-19(13-15-21)16-20(17-30)29-27(31)32-18-26-24-10-6-4-8-22(24)23-9-5-7-11-25(23)26/h4-15,20,26,30H,16-18H2,1-3H3,(H,29,31)/t20-/m0/s1
InChI Key
OCTLGTZNAJNVHZ-FQEVSTJZSA-N
Canonical SMILES
CC(C)(C)OC1=CC=C(C=C1)CC(CO)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
1. Vanadyl complexes bearing bi-dentate phenoxyimine ligands: synthesis, structural studies and ethylene polymerization capability
Jing Ma, Ke-Qing Zhao, Mark J Walton, Joseph A Wright, Josef W A Frese, Mark R J Elsegood, Qifeng Xing, Wen-Hua Sun, Carl Redshaw Dalton Trans. 2014 Jun 14;43(22):8300-10. doi: 10.1039/c4dt00021h.
Reaction of [VO(OnPr)3] with the Schiff bases 3,5-(tBu)2-2-OH-C6H2CH(N(x-OR-C6H4)) (R = Me; x = 2, L(1)H; x = 3, L(2)H; x = 4, L(3)H; R = Et (L(4)H), CF3 (L(5)H), Ph (L(6)H)) or 4-methyl-3-(R)-2-(OH)-C6H4C[double bond, length as m-dash]N(2'-(2''-(OR1)C6H4)C6H4) (R = adamantyl, R(1) = Ph (L(7)H) or R = C(Me)2Ph, R(1) = Ph (L(8)H)) afforded the bis(chelate) vanadium(iv) complexes [VO(L(n))2] (n = 1 (1·2MeCN); n = 2 (2); n = 3 (3·2MeCN); n = 4 (4); n = 5 (5); n = 6 (6); n = 6, (7·1.5MeCN); n = 7, (8); n = 8, (9)); in the case of L(6)H, the oxo-bridged vanadium(v) complexes [VO(μ-O)(L(6))]2 (10) was also isolated. By contrast, interaction of 4-methyl-3-(R)-2-(OH)-C6H4C[double bond, length as m-dash]N(2'-(2''-(OR1)C6H4)C6H4) (R = adamantyl, R(1) = Me (L(9)H); R = tBu, R(1) = Me (L(10)H); R = C(Me)2Ph, R(1) = Me (L(11)H)) with [VO(OnPr)3] led to the isolation of the dinuclear complexes [VO(μ-OH)(μ-OnPr)(L(n))]2 (n = 9, (·4MeCN); 10, (12); 11, (13)), respectively. The molecular structures of 1 to 13 are reported. All complexes have been screened as pre-catalysts for the polymerization of ethylene in the presence of the co-catalyst diethylaluminium chloride (DEAC) with or without ethyltrichloroacetate (ETA) present at 1 or 10 bar of ethylene. Under high pressure, all pre-catalysts exhibited high activity and afforded high molecular weight (Mw ≈ 200 000 to 675 000 g mol(-1)), linear polyethylene with activities (in the presence of ETA) in the range 4960-16 400 g mmol(-1) h(-1); at one bar, the products were generally of lower molecular weight. The use of methylaluminoxane (MAO) or modified MAO (MMAO) as co-catalyst led to trace or poor (≤110 g mmol(-1) h(-1)) activity, respectively.
2. Synthesis and structure of a new bulky bis-(alkoxide) ligand on a terphenyl platform
Sudheer S Kurup, Sandra Nasser, Cassandra L Ward, Stanislav Groysman Acta Crystallogr E Crystallogr Commun. 2022 Jan 1;78(Pt 1):92-96. doi: 10.1107/S2056989021013438.
A new sterically bulky chelating bis-(alkoxide) ligand 3,3'-([1,1':4',1''-terphen-yl]-2,2''-di-yl)bis-(2,2,4,4-tetra-methyl-pentan-3-ol), (H2[OO]tBu), was prepared in a two-step process as the di-chloro-methane monosolvate, C36H50O2·CH2Cl2. The first step is a Suzuki-Miyaura coupling reaction between 2-bromo-phenyl-boronic acid and 1,4-di-iodo-benzene. The resulting 2,2''-di-bromo-1,1':4',1''-terphenyl was reacted with t BuLi and hexa-methyl-acetone to obtain the desired product. The crystal structure of H2[OO]tBu revealed an anti conformation of the [CPh2(OH)] fragments relative to the central phenyl. Furthermore, the hydroxyl groups point away from each other. Likely because of this anti-anti conformation, the attempts to synthesize first-row transition-metal complexes with H2[OO]tBu were not successful.
3. Sterically directed nitronate complexes of 2,6-di-tert-butyl-4-nitrophenoxide with Cu(ii) and Zn(ii) and their H-atom transfer reactivity
Thomas R Porter, Ellen C Hayes, Werner Kaminsky, James M Mayer Dalton Trans. 2017 Feb 21;46(8):2551-2558. doi: 10.1039/c6dt04427a.
The bulky 2,6-di-tert-butyl-4-nitrophenolate ligand forms complexes with [TptBuCuII]+ and [TptBuZnII]+ binding via the nitro group in an unusual nitronato-quinone resonance form (TptBu = hydro-tris(3-tert-butyl-pyrazol-1-yl)borate). The Cu complex in the solid state has a five-coordinate κ2-nitronate structure, while the Zn analogue has a four-coordinate κ1-nitronate ligand. 4-Nitrophenol, without the 2,6-di-tert-butyl substituents, instead binds to [TptBuCuII]+ through the phenolate oxygen. This difference in binding is very likely due to the steric difficulty in binding a 2,6-di-tert-butyl-phenolate ligand to the [TptBuMII]+ unit. TptBuCuII(κ2-O2NtBu2C6H2O) reacts with the hydroxylamine TEMPO-H (2,2,6,6-tetramethylpiperidin-1-ol) by abstracting a hydrogen atom. This system thus shows an unusual sterically enforced transition metal-ligand binding motif and a copper-phenolate interaction that differs from what is typically observed in biological and chemical catalysis.
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