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[T.-BU-C=C(ME)CHC(ME)N(AR)]-V=NAR(OTF)

Compound with spectra: 3 NMR

[T.-BU-C=C(ME)CHC(ME)N(AR)]-V=NAR(OTF)
SpectraBase Compound ID 229TzrfPEFF
InChI InChI=1S/C22H33N.C12H17N.CHF3O3S.V/c1-15(2)19-11-10-12-20(16(3)4)21(19)23-18(6)13-17(5)14-22(7,8)9;1-8(2)10-6-5-7-11(9(3)4)12(10)13;2-1(3,4)8(5,6)7;/h10-13,15-16H,1-9H3;5-9H,1-4H3;(H,5,6,7);/q-1;;;+2/p-1/b17-14?,18-13-;;;
InChIKey ZWROZLVAHSWBGV-QCHUIQTHSA-M
Mol Weight 686.79 g/mol
Molecular Formula C35H50F3N2O3SV
Exact Mass 686.293381 g/mol
Parent InChIKey MDNZBNNHPMCHHE-XCQOPTFXSA-M

View Spectrum of [T.-BU-C=C(ME)CHC(ME)N(AR)]-V=NAR(OTF)

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent TOLUENE-D8

View Spectrum of [T.-BU-C=C(ME)CHC(ME)N(AR)]-V=NAR(OTF)

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent TOLUENE-D8

View Spectrum of [T.-BU-C=C(ME)CHC(ME)N(AR)]-V=NAR(OTF)

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent TOLUENE-D8
benzenamine, N-[(11Z)-3-methyl-11H-indeno[1,2-b]quinolin-11-ylidene]-
3-Methyl-5-(4-propoxy-phenyl)-1,2,3,4-tetrahydro-benzo[a]phenanthridine
4-thiazolidinone, 5-(5-chloro-3-methyl-2(3H)-benzothiazolylidene)-3-ethyl-2-(6-quinolinylimino)-, (2Z,5Z)-
2-Phenyl-6-diethylamino-5-methyl-1-(2,4,6-trimethyl-phenyl)-4,4-bis(trifluoromethyl)-1,4-dihydro-pyrimidine
(2E,5Z)-3-butyl-5-(5-chloro-3-ethyl-1,3-benzothiazol-2(3H)-ylidene)-2-{[(E)-1-phenylethyl]imino}-1,3-thiazolidin-4-one
3-pyridinecarboxamide, 4-(2-chlorophenyl)-5-cyano-1,4-dihydro-2-methyl-6-[[2-oxo-2-(phenylamino)ethyl]thio]-N-phenyl-
1-[3-amino-4-(3-methoxyphenyl)-6-phenylthieno[2,3-b]pyridin-2-yl]-2,2,2-trifluoroethanone
2-Diazanyl-3-(4-methylphenyl)-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-4-one
OOPODIN
3-Methyl-5-p-phenetyl-1,2,3,4-tetrahydrobenzo[a]phenanthridine
Title Journal or Book Year
Terminal Vanadium−Neopentylidyne Complexes and Intramolecular Cross-Metathesis Reactions to Generate Azametalacyclohexatrienes Journal of the American Chemical Society 2004
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