Month: November 2022

On November 15, 2013, Romero-Estudillo, Ivan; Boto, Alicia published an article.Synthetic Route of 14602-86-9 The title of the article was Creating diversity by site-selective peptide modification: A customizable unit affords amino acids with high optical purity. And the article contained the following:

The development of peptide libraries by site-selective modification of a few parent peptides would save valuable time and materials in discovery processes, but still is a difficult synthetic challenge. Herein natural hydroxyproline is introduced as a “convertible” unit for the production of a variety of optically pure amino acids, including expensive N-alkyl amino acids, and to achieve the mild, efficient, and site-selective modification of peptides. The experimental process involved the reaction of (1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl carbonochloridate(cas: 14602-86-9).Synthetic Route of 14602-86-9

The Article related to hydroxyproline amino acid regioselective synthesis tandem radical scission oxidation, oxo homoalanine reductive amination lactamization horner wadsworth emmons reaction, peptide synthesis hydroxyproline reduction alkylation and other aspects.Synthetic Route of 14602-86-9

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Hurst, Timothy E.; Taylor, Richard J. K. published an article in 2017, the title of the article was A Cu-Catalysed Radical Cross-Dehydrogenative Coupling Approach to Acridanes and Related Heterocycles.Electric Literature of 14602-86-9 And the article contains the following content:

The synthesis of acridanes and related compounds through a Cu-catalyzed radical cross-dehydrogenative coupling of simple 2-[2-(arylamino)aryl]malonates is reported. This method can be further streamlined to a one-pot protocol involving the in situ formation of the 2-[2-(arylamino)aryl]malonate by α-arylation of di-Et malonate with 2-bromodiarylamines under Pd catalysis, followed by Cu-catalyzed cyclization. The experimental process involved the reaction of (1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl carbonochloridate(cas: 14602-86-9).Electric Literature of 14602-86-9

The Article related to acridane derivative preparation, arylaminophenylmalonate preparation dehydrogenative coupling copper catalyst, acridanes, copper, cross‐coupling, dehydrogenation, homogeneous catalysis, nitrogen heterocycles, one‐pot reaction and other aspects.Electric Literature of 14602-86-9

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

On July 20, 2020, Plaza, Manuel; Jandl, Christian; Bach, Thorsten published an article.COA of Formula: C7H11ClO3 The title of the article was Photochemical Deracemization of Allenes and Subsequent Chirality Transfer. And the article contained the following:

Trisubstituted allenes with a 3-(1′-alkenylidene)-pyrrolidin-2-one motif were successfully deracemized (13 examples, 86-98% ee) employing visible light (λ=420 nm) and a chiral triplet sensitizer as the catalyst (2.5 mol %). The photocatalyst likely operates by selective recognition of one allene enantiomer via hydrogen bonds and by a triplet-sensitized racemization process. Even a tetrasubstituted allene (45% ee) and a seven-membered 3-(1′-alkenylidene)-azepan-2-one (62% ee) could be enantiomerically enriched under the chosen conditions. It was shown that the axial chirality of the allenes can be converted into point chirality by a Diels-Alder (94-97% ee) or a bromination reaction (91% ee). Ring opening of the five-membered pyrrolidin-2-one was achieved without significantly compromising the integrity of the chirality axis (92% ee). The experimental process involved the reaction of Methyl 6-chloro-6-oxohexanoate(cas: 35444-44-1).COA of Formula: C7H11ClO3

The Article related to allene deracemization chiral resolution chiral triplet sensitizer enantioselectivity light, chiral trisubstituted allene preparation, allenes, chiral resolution, enantioselectivity, hydrogen bonds, photochemistry, sensitizers and other aspects.COA of Formula: C7H11ClO3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

On December 31, 1979, Corley, L. S.; Vogl, O. published an article.Application In Synthesis of trimethyloxosulphonium chloride The title of the article was Haloaldehyde polymers. 16. Stabilization of anionically-prepared polychloral by end-capping with decomposable cations and other additives. And the article contained the following:

Completely or partially stable polychloral [25154-92-1] was obtained by anionic cryotachensic polymerization of Cl3CCHO in the presence of alkylating or acylating agents, e.g. Me2SO4 [77-78-1]. Stabilization was also effected by polymerization using salts with easily decomposed cations as anionic initiators. Sulfonium salts, e.g. Me3S+Cl- [3086-29-1] and [Me2S+CH2Ph]Br- [14182-15-1], and iodonium salts, e.g. Ph2I+Cl- [1483-72-3], were effective although quant. stabilization was not achieved. Polychloral with improved stability was also obtained using certain amide acetals, e.g. Me2NCH(OMe)2 [4637-24-5], as initiators. The experimental process involved the reaction of trimethyloxosulphonium chloride(cas: 5034-06-0).Application In Synthesis of trimethyloxosulphonium chloride

The Article related to polychloral stabilization, chloral anionic polymerization stability, sulfonium catalyst chloral polymerization, iodonium initiator chloral polymerization, amide acetal chloral polymerization, end capping polychloral stability and other aspects.Application In Synthesis of trimethyloxosulphonium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

On April 30, 2016, Al-Ghorbani, Mohammed; Pavankumar, G. S.; Naveen, P.; Thirusangu, Prabhu; Prabhakar, B. T.; Khanum, Shaukath Ara published an article.COA of Formula: C7H4ClNO4 The title of the article was Synthesis and an angiolytic role of novel piperazine-benzothiazole analogues on neovascularization, a chief tumoral parameter in neoplastic development. And the article contained the following:

A novel series of benzoic acid N’-[2-(4-benzothiazol-2-yl-piperazin-1-yl)-acetyl]-hydrazides (6a-j) were synthesized and characterized by IR, 1H, 13C NMR, elemental and mass spectral analyses. The in-vitro cytotoxicity and cell viability assay of the synthesized compounds 6a-j were evaluated against Dalton’s lymphoma ascites (DLA) cells. The authors’ results showed that compound 3-bromobenzoic acid N’-[2-(4-benzothiazol-2-yl-piperazin-1- yl)-acetyl]-hydrazide (6c) with a bromo group on Ph ring has showed promising antiproliferative efficacy. Further investigation of compound (6c) on in-vivo treatment model depicts the increased tumor suppression through inhibition of angiogenesis. The experimental process involved the reaction of 2-Chloro-4-nitrobenzoic acid(cas: 99-60-5).COA of Formula: C7H4ClNO4

The Article related to piperazine benzothiazole analog preparation antitumor neovascularization structure activity, antiproliferative angiogenesis piperazine benzothiazole analog, angiogenesis, antiproliferative, dla cells, piperazine–benzothiazole and other aspects.COA of Formula: C7H4ClNO4

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

On August 1, 2018, Zhou, Qian; You, Chaoqun; Zheng, Cong; Gu, Yawen; Gu, Hongchao; Zhang, Rui; Wu, Hongshuai; Sun, Baiwang published an article.Quality Control of 2-Chloro-4-nitrobenzoic acid The title of the article was 3-Nitroacridine derivatives arrest cell cycle at G0/G1 phase and induce apoptosis in human breast cancer cells may act as DNA-target anticancer agents. And the article contained the following:

DNA is considered to be one of the most promising targets for anticancer agents. Acridine analogs have anticancer activity based on DNA binding and topoisomerases inhibition. However, due to the side effects, resistance and low bioavailability, a few have entered into clin. usage and the mechanisms of action are not fully understood. Novel acridine derivatives are needed for effective cancer therapy. A series of novel 3-nitroacridine-based derivatives were synthesized, their DNA binding and anticancer activities were evaluated. The chem. modifications at position 9 of the 3-nitroacridine were crucial for DNA affinity, thus optimizing anticancer activity. UV-Vis and CD (CD) spectroscopy indicated interaction of compounds with DNA, and the binding modes were intercalation and groove binding. MTT assay and clonogenic assay showed that compounds 1, 2 and 3 had obvious cell growth inhibition effect. They induced cell apoptosis in human breast cancer cells in a dose-dependent manner, and exhibited anticancer effect via DNA damage as well as cell cycle arrest at G0/G1 phage. Using confocal fluorescent microscope, the apoptotic features were observed The results suggested that compounds 1-3 with high DNA binding affinity and good inhibitory effect of cancer cell proliferation can be developed as prime candidates for further chem. optimization. The experimental process involved the reaction of 2-Chloro-4-nitrobenzoic acid(cas: 99-60-5).Quality Control of 2-Chloro-4-nitrobenzoic acid

The Article related to breast cancer dna target anticancer agent 3 nitroacridine derivative, apoptosis cell cycle arrest g1 g0 phase, acridine derivatives, anticancer activity, apoptosis, dna binding, structure-activity relationship (sar), synthesis and other aspects.Quality Control of 2-Chloro-4-nitrobenzoic acid

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

On November 15, 2019, De Luca, Stefania; Digilio, Giuseppe; Verdoliva, Valentina; Tovillas, Pablo; Jimenez-Oses, Gonzalo; Peregrina, Jesus M. published an article.Category: chlorides-buliding-blocks The title of the article was Lanthionine peptides by S-alkylation with substituted cyclic sulfamidates promoted by activated molecular sieves: Effects of the sulfamidate structure on the yield. And the article contained the following:

A green and efficient method for preparing lanthionine peptides by a highly chemoselective and stereochem. controlled procedure is presented. It involves an S-alkylation reaction, promoted by activated mol. sieves, on chiral cyclic sulfamidates, both N-protected and unprotected. Of note, the reaction yield was high also for cyclic sulfamidates bearing a free amine group, while other strategies failed to achieve a ring-opening nucleophilic reaction with N-unprotected substrates. To prove the feasibility of the procedure, the synthesis of a thioether ring B mimetic of the natural lantibiotic haloduracin β was performed. The experimental process involved the reaction of tert-Butyl trichloroacetimidate(cas: 98946-18-0).Category: chlorides-buliding-blocks

The Article related to lanthionine peptide enantioselective synthesis green chem, solid phase peptide synthesis, chiral cyclic sulfamidate s alkylation thioetherification cyclization, thioether ring b preparation natural lantibiotic beta haloduracin and other aspects.Category: chlorides-buliding-blocks

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

On September 8, 2016, Masuda, Yuichi; Maruyama, Chitose; Kawabata, Kyuichi; Hamano, Yoshimitsu; Doi, Takayuki published an article.Application of 98946-18-0 The title of the article was Synthesis of (2S,3R,4R)-3,4-dihydroxyarginine and its inhibitory activity against nitric oxide synthase. And the article contained the following:

A synthesis of (2S,3R,4R)-3,4-dihydroxyarginine, a metabolic intermediate of streptothricin, was accomplished. The (3R,4R)-dihydroxy groups were constructed by asym. syn-dihydroxylation of (E)-alkene, which was obtained by cross-metathesis of allylamine and L-vinylglycine derivatives The synthesis of (2S,3S,4S)-3,4-dihydroxyarginine was also achieved in the same manner. The (2S,3R,4R)-3,4-dihydroxyarginine exhibited inhibitory activity against inducible nitric oxide synthase, unlike (2S,3S,4S)-3,4-dihydroxyarginine. The experimental process involved the reaction of tert-Butyl trichloroacetimidate(cas: 98946-18-0).Application of 98946-18-0

The Article related to arginine dihydroxy enantioselective diastereoselective synthesis metabolic intermediate streptothricin, nitric oxide synthase inhibitor dihydroxyarginine, allylamine vinylglycine cross metathesis alkene asym syn dihydroxylation and other aspects.Application of 98946-18-0

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

On November 7, 2007, Kakei, Hiroyuki; Sone, Toshihiko; Sohtome, Yoshihiro; Matsunaga, Shigeki; Shibasaki, Masakatsu published an article.HPLC of Formula: 5034-06-0 The title of the article was Catalytic Asymmetric Cyclopropanation of Enones with Dimethyloxosulfonium Methylide Promoted by a La-Li3-(Biphenyldiolate)3 + NaI Complex. And the article contained the following:

Catalytic asym. cyclopropanation of enones with dimethyloxosulfonium methylide using a La-Li3-(biphenyldiolate)3 + NaI complex is described. The present method is complementary to the previously reported catalytic enantioselective methods in terms of ylides used, and trans products, e.g., I, were exclusively obtained in good yield (96-73%) and high enantioselectivity (99-84% ee). Use of biphenyldiol and NaI additive was essential to achieve high enantioselectivity. The experimental process involved the reaction of trimethyloxosulphonium chloride(cas: 5034-06-0).HPLC of Formula: 5034-06-0

The Article related to enone dimethyloxosulfonium methylide lanthanium chiral biphenyldiol complex asym cyclopropanation, cyclopropyl ketone derivative stereoselective preparation, asym cyclopropanation catalyst lanthanium chiral biphenyldiol complex and other aspects.HPLC of Formula: 5034-06-0

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

On March 28, 2021, Andrade-Sampedro, Paula; Matxain, Jon M.; Correa, Arkaitz published an article.Category: chlorides-buliding-blocks The title of the article was Pd-Catalyzed C(sp2)-H Alkoxycarbonylation of Phenethyl- and Benzylamines with Chloroformates as CO Surrogates. And the article contained the following:

Herein, an unprecedented Pd-catalyzed C(sp2)-H alkoxycarbonylation of phenylalanine derivatives and other amines featuring picolinamide as the directing group (DG) to afford the corresponding alkoxycarbonylated products, e.g., I (R = H, CO2Et), is reported. This oxidative coupling is distinguished by its scalability, operational simplicity, and avoids the use of toxic carbon monoxide as the C1 source. Remarkably, the easy cleavage of the DG enabled the efficient assembly of isoindolinone compounds D. Functional Theory calculations support a PdII/PdIV catalytic cycle. The experimental process involved the reaction of (1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl carbonochloridate(cas: 14602-86-9).Category: chlorides-buliding-blocks

The Article related to alkoxycarbonylated phenylalanine derivative site selective preparation, phenylalanine chloroformate alkoxycarbonylation palladium catalyst, c−h functionalization, dft calculations, alkoxycarbonylation, benzylamine, phenylalanine and other aspects.Category: chlorides-buliding-blocks

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics