Category: 156311-83-0

Total synthesis of halipeptins A and D and analogues was written by Nicolaou, K. C.;Kim, David W.;Schlawe, Daniel;Lizos, Dimitrios E.;de Noronha, Rita G.;Longbottom, Deborah A.. And the article was included in Angewandte Chemie, International Edition in 2005.Category: triazoles The following contents are mentioned in the article:

Deceptive rings: Halipeptins A I (R² = CH₂OH) and D I (R² = Me) and analogs thereof were synthesized from azide fragment II and ester fragment III (R = OSiPh₂CMe₃, H, resp.). Key steps included peptide-bond formation, DAST-induced thiazoline construction, and macrolactamization. Unlike the naturally isolated (and possibly contaminated) material, synthetic halipeptin D exhibited only weak toxicity against tumor cells. This study involved multiple reactions and reactants, such as ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0Category: triazoles).

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. Triazoles are important five-member nitrogen heterocycles involved in a wide range of industrial applications such as agrochemicals, corrosion inhibitors, dyes, optical brighteners, as well as biologically active agents. 1,2,3-Triazoles are usually prepared following (3+2) cycloaddition protocols. A common technique for unsubstituted triazoles is the Huisgen azide-alkyne 1,3-dipolar cycloaddition: a azide and an alkyne react at high temperature to form a ring. However, the Huisgen strategy produces a mixture of isomers (typically 1,4- and 1,5-disubstituted) when used to produce substituted triazoles.Category: triazoles

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Heteroaryl ethers by oxidative palladium catalysis of pyridotriazol-1-yloxy pyrimidines with arylboronic acids was written by Bardhan, Sujata;Wacharasindhu, Sumrit;Wan, Zhao-Kui;Mansour, Tarek S.. And the article was included in Organic Letters in 2009.Formula: C17H27F6N7OP2 The following contents are mentioned in the article:

The oxidative palladium-catalyzed cross-coupling of pyrimidines containing pyridotriazol-1-yloxy (OPt) as either a urea or an amide functional group with arylboronic acids in the presence of Cs₂CO₃ in DME containing 0.6-1.0% H₂O is described for the preparation of heteroaryl ethers. The bromo substitution in the case of 3-(5-bromo-pyrimidin-2-yloxy)-3H-[1,2,3]triazolo[4,5-b]pyridine could serve as a handle for further elaborations such as Suzuki coupling for attaching varied aryl groups. This study involved multiple reactions and reactants, such as ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0Formula: C17H27F6N7OP2).

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. However, triazoles are also useful in bioorthogonal chemistry, because the large number of nitrogen atoms causes triazoles to react similar to azides.Triazole heterocyclic structures are found to form many weak nonbond interactions with the receptors and enzymes in biological systems.Formula: C17H27F6N7OP2

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Redox-gated electron transport in electrically wired ferrocene molecules was written by Xiao, Xiaoyin;Brune, Daniel;He, Jin;Lindsay, Stuart;Gorman, Christopher B.;Tao, Nongjian. And the article was included in Chemical Physics in 2006.Formula: C17H27F6N7OP2 The following contents are mentioned in the article:

We have synthesized cysteamine-terminated ferrocene mols. and determined the dependence of the electron transport properties of the mols. on their redox states by measuring the current through the mols. as a function of the electrode potential. The current fluctuates over a large range, but its average value increases with the potential. We attribute the current fluctuation and its increase with the potential to the switching of the mols. from low-conductance reduced state to high-conductance oxidized state. This study involved multiple reactions and reactants, such as ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0Formula: C17H27F6N7OP2).

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. The triazole ring is a relatively stable functional group, and the triazole bond can be used for a variety of applications, such as replacing the phosphate backbone of DNA. 1,2,3-Triazoles are usually prepared following (3+2) cycloaddition protocols. A common technique for unsubstituted triazoles is the Huisgen azide-alkyne 1,3-dipolar cycloaddition: a azide and an alkyne react at high temperature to form a ring. However, the Huisgen strategy produces a mixture of isomers (typically 1,4- and 1,5-disubstituted) when used to produce substituted triazoles.Formula: C17H27F6N7OP2

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Synthesis of vaniprevir (MK-7009): Lactamization to prepare a 20-membered macrocycle was written by Song, Zhiguo J.;Tellers, David M.;Journet, Michel;Kuethe, Jeffrey T.;Lieberman, David;Humphrey, Guy;Zhang, Fei;Peng, Zhihui;Waters, Marjorie S.;Zewge, Daniel;Nolting, Andrew;Zhao, Dalian;Reamer, Robert A.;Dormer, Peter G.;Belyk, Kevin M.;Davies, Ian W.;Devine, Paul N.;Tschaen, David M.. And the article was included in Journal of Organic Chemistry in 2011.Formula: C17H27F6N7OP2 The following contents are mentioned in the article:

Development of a practical synthesis of MK-7009 I, a 20-membered macrocycle, is described. A variety of ring-closing strategies were evaluated, including ring-closing metathesis, intermol. palladium-catalyzed cross-couplings, and macrolactamization. Ring closure via macrolactamization was found to give the highest yields under relatively high reaction concentrations Optimization of the ring formation step and the synthesis of key intermediates en route to MK-7009 are reported. This study involved multiple reactions and reactants, such as ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0Formula: C17H27F6N7OP2).

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. Triazoles are important five-member nitrogen heterocycles involved in a wide range of industrial applications such as agrochemicals, corrosion inhibitors, dyes, optical brighteners, as well as biologically active agents. Many triazoles have antifungal effects: the triazole antifungal drugs include fluconazole, isavuconazole, itraconazole, voriconazole, pramiconazole, ravuconazole, and posaconazole and triazole plant-protection fungicides include epoxiconazole, triadimenol, myclobutanil, propiconazole, prothioconazole, metconazole, cyproconazole, tebuconazole, flusilazole and paclobutrazol.Formula: C17H27F6N7OP2

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Pyrrolidide formation as a side reaction during activation of carboxylic acids by phosphonium salt coupling reagents was written by Alsina, Jordi;Barany, George;Albericio, Fernando;Kates, Steven A.. And the article was included in Letters in Peptide Science in 1999.SDS of cas: 156311-83-0 The following contents are mentioned in the article:

Pyrrolidide derivatives are observed as unwanted byproducts from slow reactions of activated carboxylates with nucleophilic amines, as mediated by phosphonium salt coupling reagents (PyAOP, PyBOP, PyBroP). This side reaction is attributed to the presence of small amounts (e.g., 0.5%, weight/weight) of pyrrolidine as a contaminant to com. phosphonium salts, and does not occur when the reagents are crystallized before their use in coupling reactions. This study involved multiple reactions and reactants, such as ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0SDS of cas: 156311-83-0).

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. Triazoles consist of a five-membered ring containing three nitrogen atoms and are biologically active, especially as antifungal, antimicrobial and enzyme inhibitors.Triazole heterocyclic structures are found to form many weak nonbond interactions with the receptors and enzymes in biological systems.SDS of cas: 156311-83-0

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

On the use of PyAOP, a phosphonium salt derived from HOAt, in solid-phase peptide synthesis was written by Albericio, Fernando;Cases, Marta;Alsina, Jordi;Triolo, Salvatore A.;Carpino, Louis A.;Kates, Steven A.. And the article was included in Tetrahedron Letters in 1997.Application of 156311-83-0 The following contents are mentioned in the article:

Phosphonium derivatives of HOAt such as PyAOP (I) are useful for the solid-phase preparation of a range of peptides that include those incorporating hindered amino acids, difficult short sequences, and cyclic peptides. An advantage relative to uronium salts is that excess PyAOP does not undergo the detrimental side-reaction at the amino terminus which blocks further chain assembly. This study involved multiple reactions and reactants, such as ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0Application of 156311-83-0).

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. Triazoles consist of a five-membered ring containing three nitrogen atoms and are biologically active, especially as antifungal, antimicrobial and enzyme inhibitors. 1,2,3-Triazoles are usually prepared following (3+2) cycloaddition protocols. A common technique for unsubstituted triazoles is the Huisgen azide-alkyne 1,3-dipolar cycloaddition: a azide and an alkyne react at high temperature to form a ring. However, the Huisgen strategy produces a mixture of isomers (typically 1,4- and 1,5-disubstituted) when used to produce substituted triazoles.Application of 156311-83-0

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Rational design of a fluopyram hapten and preparation of bioconjugates and antibodies for immunoanalysis was written by Ceballos-Alcantarilla, E.;Agullo, C.;Abad-Fuentes, A.;Abad-Somovilla, A.;Mercader, J. V.. And the article was included in RSC Advances in 2015.Recommanded Product: 156311-83-0 The following contents are mentioned in the article:

A fluopyram hapten was designed in which insignificant electronic and structural modifications were foreseen and all potentially interacting chem. moieties were maintained. This hapten was prepared by total synthesis and three immunol. active bioconjugates were obtained and characterized. High-affinity and specific antibodies to fluopyram were raised. This study involved multiple reactions and reactants, such as ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0Recommanded Product: 156311-83-0).

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. Triazoles consist of a five-membered ring containing three nitrogen atoms and are biologically active, especially as antifungal, antimicrobial and enzyme inhibitors. Due to the structural characteristics, both 1,2,3- and 1,2,4-triazoles are able to accommodate a broad range of substituents (electrophiles and nucleophiles) around the core structures and pave the way for the construction of diverse novel bioactive molecules.Recommanded Product: 156311-83-0

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Solid-phase modular synthesis of park nucleotide and lipids I and II analogues was written by Katsuyama, Akira;Sato, Kousuke;Yakushiji, Fumika;Matsumaru, Takanori;Ichikawa, Satoshi. And the article was included in Chemical & Pharmaceutical Bulletin in 2018.SDS of cas: 156311-83-0 The following contents are mentioned in the article:

A solid-phase synthesis of Park nucleotide as well as lipids I and II analogs, which is applicable to the synthesis of a range of analogs, is described in this work. This technique allows highly functionalized macromols. to he modularly labeled. Multiple steps are used in a short time (4d) with a single purification step to synthesize the mols. by solid-phase synthesis. This study involved multiple reactions and reactants, such as ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0SDS of cas: 156311-83-0).

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. The many free lone pairs in triazoles make them useful as coordination compounds, although not typically as haptic ligands. Many triazoles have antifungal effects: the triazole antifungal drugs include fluconazole, isavuconazole, itraconazole, voriconazole, pramiconazole, ravuconazole, and posaconazole and triazole plant-protection fungicides include epoxiconazole, triadimenol, myclobutanil, propiconazole, prothioconazole, metconazole, cyproconazole, tebuconazole, flusilazole and paclobutrazol.SDS of cas: 156311-83-0

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Microwave-assisted coupling of carboxylic acids to a polymer bound hydrazine linker was written by Lindquist, Charlotta;Tedebark, Ulf;Ersoy, Oguz;Somfai, Peter. And the article was included in Synthetic Communications in 2003.Synthetic Route of C17H27F6N7OP2 The following contents are mentioned in the article:

A set of carboxylic acids, all being potential scaffolds for combinatorial chem. or peptide synthesis, were coupled to a polymer bound aryl hydrazine linker using microwave irradiation in good yields. Improved yields and reduced reaction times were achieved by using microwave-assisted heating compared to conventional heating. This study involved multiple reactions and reactants, such as ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0Synthetic Route of C17H27F6N7OP2).

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. Many triazoles are versatile, biologically active compounds commonly used as fungicides and plant retardants. Triazole growth retardants such as uniconazole and paclobutrazol have been known to inhibit the biosynthesis of gibberellins by blocking kaurene oxidase, an P450 enzymeSynthetic Route of C17H27F6N7OP2

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Synthesis of vaniprevir (MK-7009): Lactamization to prepare a 20-membered macrocycle [Erratum to document cited in CA155:407318] was written by Song, Zhiguo J.;Tellers, David M.;Journet, Michel;Kuethe, Jeffrey T.;Lieberman, David;Humphrey, Guy;Zhang, Fei;Peng, Zhihui;Waters, Marjorie S.;Zewge, Daniel;Nolting, Andrew;Zhao, Dalian;Reamer, Robert A.;Dormer, Peter G.;Belyk, Kevin M.;Davies, Ian W.;Devine, Paul N.;Tschaen, David M.. And the article was included in Journal of Organic Chemistry in 2011.SDS of cas: 156311-83-0 The following contents are mentioned in the article:

On page 7804, the title, the first sentence of the Abstract and, the second paragraph of the Introduction contained an error; the correction is given. On page 7805, the paragraph headed with “Palladium-Mediated Macrocyclization” contained a text error; the correction is given. This study involved multiple reactions and reactants, such as ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0SDS of cas: 156311-83-0).

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. The triazole ring is a relatively stable functional group, and the triazole bond can be used for a variety of applications, such as replacing the phosphate backbone of DNA. Due to the structural characteristics, both 1,2,3- and 1,2,4-triazoles are able to accommodate a broad range of substituents (electrophiles and nucleophiles) around the core structures and pave the way for the construction of diverse novel bioactive molecules.SDS of cas: 156311-83-0

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics