Wang, Tong-Tong’s team published research in Organic Letters in 23 | CAS: 1076-59-1

Organic Letters published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C7H6ClF3N2, HPLC of Formula: 1076-59-1.

Wang, Tong-Tong published the artcileRh(III)-Catalyzed Regioselective Annulations of 3-Arylisoxazolones and 3-Aryl-1,4,2-dioxazol-5-ones with Propargyl Alcohols: Access to 4-Arylisoquinolines and 4-Arylisoquinolones, HPLC of Formula: 1076-59-1, the publication is Organic Letters (2021), 23(15), 5952-5957, database is CAplus and MEDLINE.

The Rh(III)-catalyzed dual directing group assisted C-H activation/annulation of 3-arylisoxazolones with propargyl alcs. were developed, which expanded the application scope of isoxazolones in organic synthesis. This protocol also worked well with 3-aryl-1,4,2-dioxazol-5-ones to produce synthetically and biol. important 4-arylisoquinolones.

Organic Letters published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C7H6ClF3N2, HPLC of Formula: 1076-59-1.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Hallen, K.’s team published research in Acta Anaesthesiologica Scandinavica in 62 | CAS: 198470-85-8

Acta Anaesthesiologica Scandinavica published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C19H17N2NaO4S, Application In Synthesis of 198470-85-8.

Hallen, K. published the artcileIsocapnic hyperventilation provides early extubation after head and neck surgery: A prospective randomized trial, Application In Synthesis of 198470-85-8, the publication is Acta Anaesthesiologica Scandinavica (2018), 62(8), 1064-1071, database is CAplus and MEDLINE.

Background : Isocapnic hyperventilation (IHV) shortens recovery time after inhalation anesthesia by increasing ventilation while maintaining a normal airway carbon dioxide (CO2)-level. One way of performing IHV is to infuse CO2 to the inspiratory limb of a breathing circuit during mech. hyperventilation (HV). In a prospective randomized study, we compared this IHV technique to a standard emergence procedure (control). Methods : Thirty-one adult ASA I-III patients undergoing long-duration (>3 h) sevoflurane anesthesia for major head and neck surgery were included and randomized to IHV-treatment (n = 16) or control (n = 15). IHV was performed at minute ventilation 13.6 ± 4.3 L/min and CO2 delivery, dosed according to a nomogram tested in a pilot study. Time to extubation and eye-opening was recorded. Inspired (FICO2) and expired (FETCO2) CO2 and arterial CO2 levels (PaCO2) were monitored. Cognition was tested preoperatively and at 20, 40 and 60 min after surgery. Results : Time from turning off the vaporizer to extubation was 13.7 ± 2.5 min in the IHV group and 27.4 ± 6.5 min in controls (P < .001). Two minutes after extubation, PaCO2 was 6.2 ± 0.5 and 6.2 ± 0.6 kPa in the IHV and control group resp. In 69% (IHV) vs 53% (controls), post-operative cognition returned to pre-operative values within 40 min after surgery (NS). Incidences of pain and nausea/vomiting did not differ between groups. Conclusions : In this randomized trial comparing an IHV method with a standard weaning procedure, time to extubation was reduced with 50% in the IHV group. The described IHV method can be used to decrease emergence time from inhalation anesthesia.

Acta Anaesthesiologica Scandinavica published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C19H17N2NaO4S, Application In Synthesis of 198470-85-8.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Qi, Suo-Suo’s team published research in Organic & Biomolecular Chemistry in 18 | CAS: 1076-59-1

Organic & Biomolecular Chemistry published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C9H7NO2, Application In Synthesis of 1076-59-1.

Qi, Suo-Suo published the artcileRegioselective catalytic asymmetric N-alkylation of isoxazol-5-ones with para-quinone methides, Application In Synthesis of 1076-59-1, the publication is Organic & Biomolecular Chemistry (2020), 18(13), 2398-2404, database is CAplus and MEDLINE.

A highly regioselective and enantioselective N-alkylation of isoxazol-5-ones with para-quinone methides promoted by bi-functional squaramide catalysts was developed. This unexpected asym. N-addition of isoxazolinones afforded a series of enantioenriched N-diarylmethane substituted isoxazolinones I (R1 = H, 2-Me, 4-CF3, etc.; R2 = H, Me, Et, Ph, Bn; R3 = Ph, 2-MeOC6H4, 2-naphthyl, etc.) with high yields and enantioselectivities (up to 97 : 3 er). This reaction not only provides a useful approach for intermol. chiral C-N bond formation but also demonstrates the immense potential of isoxazol-5-ones as N-nucleophiles in catalytic asym. reactions.

Organic & Biomolecular Chemistry published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C9H7NO2, Application In Synthesis of 1076-59-1.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Sun, Xiu-rong’s team published research in Shiyong Yaowu Yu Linchuang in 19 | CAS: 198470-85-8

Shiyong Yaowu Yu Linchuang published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C7H5ClN2S, Formula: C19H17N2NaO4S.

Sun, Xiu-rong published the artcileObservation on analgesic effect of parecoxib sodium on patients undergoing subtotal thyroidectomy, Formula: C19H17N2NaO4S, the publication is Shiyong Yaowu Yu Linchuang (2016), 19(5), 599-601, database is CAplus.

To discuss the analgesic effect of parecoxib sodium on patients who have undergone subtotal thyroidectomy. The clin. data of 105 cases who had undergone subtotal thyroidectomy in our hospital from Nov. 2014 to Nov. 2015 were collected. The patients were given i.v. injection of parecoxib sodium (40 mg) 15 min before the end of operation (group A). The patients were given i.v. injection of parecoxib sodium (40 mg) immediately after patients returned to the wards (B group). The patients were given i.v. injection of NS (2 mL) solution 15 min before the end of operation (group C). Each group included 35 cases. The visual simulation pain score (VAS score) at 0, 2, 4, 6, 12, and 24 h after returning to the ward, postoperative analgesia satisfaction rate 1 d after operation and the incidence of side effects of the three groups were observed and compared. The VAS scores of A and B groups at each time point were significantly lower than that of C group, with statistically significant difference (P < 0.05). The VAS scores of A group (0, 2 h) were lower than those of B group, with statistically significant difference (P < 0.05). The postoperative occurrence rate of side effects of the three groups had no statistical significance (P > 0.05). Application of parecoxib during or after thyroid subtotal surgery can reduce postoperative pain and increase satisfaction of analgesic effect. Moreover, application of parecoxib is safe and reliable. Giving i.v. injection of parecoxib sodium 15 min before the end of surgery is a better choice.

Shiyong Yaowu Yu Linchuang published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C7H5ClN2S, Formula: C19H17N2NaO4S.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Song, Jie’s team published research in Guoji Mazuixue Yu Fusu Zazhi in 36 | CAS: 198470-85-8

Guoji Mazuixue Yu Fusu Zazhi published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C7H6O3, Synthetic Route of 198470-85-8.

Song, Jie published the artcileEffect of parecoxib sodium on inflammatory mediator and postoperative cognitive dysfunction after laparoscopic surgery in elderly patients, Synthetic Route of 198470-85-8, the publication is Guoji Mazuixue Yu Fusu Zazhi (2015), 36(6), 493-495, 501, database is CAplus.

The effects of parecoxib Na on inflammatory mediator and postoperative cognitive dysfunction (POCD) after laparoscopy surgery in elderly patients were studied. Eighty ASA patients phys. status I or II of both sexes, aged over 65 yr, weighing 45-70 kg, undergoing laparoscopic cholecystectomy, were randomly divided into parecoxib Na (group P, n=40) and control groups (group C, n=40). The patients in group P were given i.v. parecoxib 40 mg before induction of anesthesia. Ones in group C were given equal volume normal saline instead of parecoxib. Neuropsychol. testing was performed with mini-mental state examination (MMSE) on the preoperative day, 1st and 3rd postoperative day. Venous blood samples were collected before induction of anesthesia (T0), immediately after skin incision (T1), 30 min after CO2 pneumoperitoneum (T2), at the end of operation (T3), the first day of operation (T4), the third day of operation(T5) for determination of serum concentrations of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) by enzyme linked immunosorbent assay (ELISA). The development of POCD was recorded within 3 days after surgery. Compared with preoperative 24 h [group C (28.2±1.2), group P (28.8±1.0)], the MMSE scores of resting in group C and group P were significantly reduced [(23.0±2.5), (25.0±2.8)] (P<0.05). The MMSE scores of resting in group P were more than those in group C [(25.0±2.8) vs (23.0±2.5)] (P<0.05). The development of POCD within 72 h was less than that in group C (P<0.05). Compared with group C, the serum concentrations of TNFa [(11.8±1.7), (13.8±1.3), (12.3±1.6) ng/L] and IL-6 [(11.8±1.7), (13.8±1.3), (12.3±1.6) ng/L] at T3-T5 were significantly decreased in group P (P<0.05). Compared with T0, the serum concentrations of TNF-α and IL-6 at T3-T5 were increased in two group (P<0.05). Parecoxib Na might decrease the development of POCD in elderly patients undergoing laparoscopic cholecystectomy by inhibition of inflammatory responses.

Guoji Mazuixue Yu Fusu Zazhi published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C7H6O3, Synthetic Route of 198470-85-8.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Zhang, Xinyuan’s team published research in CrystEngComm in 17 | CAS: 1076-59-1

CrystEngComm published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C10H15NO, Application In Synthesis of 1076-59-1.

Zhang, Xinyuan published the artcileIsoxazolone-based single crystals with large second harmonic generation effect, Application In Synthesis of 1076-59-1, the publication is CrystEngComm (2015), 17(38), 7316-7322, database is CAplus.

Two nonlinear optical (NLO) crystals based on the 3-phenyl-5-isoxazolone moiety, (Z)-4-(4-(dimethylamino)benzylidene)-3-phenylisoxazol-5(4H)-one (C18H16N2O2, DLS) and (Z)-4-(4-methoxybenzylidene)-3-phenylisoxazol-5(4H)-one (C17H13NO3, MLS), have been successfully grown by a slow evaporation method. The powder second-harmonic generation intensities of DLS and MLS are strong, about 2.8 and 1.5 times that of OH1, resp. Such a large SHG effect is further elucidated by structure analyses and theor. calculations The optical and thermal properties of DLS and MLS have been characterized by UV-vis absorption spectroscopy, IR spectroscopy, thermal gravimetric anal. and differential scanning calorimetry.

CrystEngComm published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C10H15NO, Application In Synthesis of 1076-59-1.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Zhang, Xinyuan’s team published research in CrystEngComm in 18 | CAS: 1076-59-1

CrystEngComm published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C10H15NO, SDS of cas: 1076-59-1.

Zhang, Xinyuan published the artcileMolecular design on isoxazolone-based derivatives with large second-order harmonic generation effect and terahertz wave generation, SDS of cas: 1076-59-1, the publication is CrystEngComm (2016), 18(20), 3667-3673, database is CAplus.

A series of 3-phenyl-5-isoxazolone and 3-methyl-5-isoxazolone-based compounds with different electron donors were synthesized. Fourteen single crystals in this family were obtained by slow evaporation Single crystal X-ray studies showed that four new 3-phenyl-5-isoxazolone-based crystals, C20H18N2O2 (PDI), C15H11NO2S (PTI), C23H15NO2 (PFI), and C17H13NO2S (PMI-(I)), belong to the noncentrosymmetric space group. The inclinations to achieve noncentrosym. space groups in the 3-phenyl-5-isoxazolone-based crystals have been confirmed by first-principles calculations Powder second harmonic generation (SHG) tests revealed that the abovementioned four acentric crystals exhibited very large SHG intensities that were about 1 to 3 times that of OH1 (a commonly used nonlinear optical crystal) under 2.09μm light. Their UV-vis absorption, diffuse reflectance spectroscopy, and thermal properties were also characterized. Moreover, widely tunable and monochromatic terahertz difference frequency generation in the 3-phenyl-5-isoxazolone-based crystal C17H13NO3 (MLS) was realized for the first time.

CrystEngComm published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C10H15NO, SDS of cas: 1076-59-1.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Wang, Yu’s team published research in Sichuan Yixue in 36 | CAS: 198470-85-8

Sichuan Yixue published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C8H14O2, Name: Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide.

Wang, Yu published the artcileAnalgesic effect of parecoxib sodium and tramadol in painless induced abortion, Name: Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, the publication is Sichuan Yixue (2015), 36(1), 100-102, database is CAplus.

Objective: To compare the effect of parecoxib sodium and tramadol in combination with propofol on postoperative analgesia in painless induced abortion. Methods: 120 Cases of pregnant women of ASA I-II grade undergoing painless induced abortion were randomly divided into three groups. P group was preoperatively injected with 40 mg of parecoxib sodium, Q group was preoperatively injected with 100 mg of tramadol, and X group was preoperatively injected with 40 mg of parecoxib sodium and 100 mg of tramadol, and all groups were treated with 1.5-2.5 mg/kg propofol for anesthesia. The intraoperative consumption of propofol, intraoperative and postoperative analgesic effect and adverse reactions in the three groups were compared. Results: The intraoperative consumption of propofol in X group was significantly lower than that in P group and Q group (P < 0.05). All groups have good intraoperative analgesic effect without statistically significant difference (P > 0.05). The uterine contraction pain VAS scores at each time point during surgery in X group were significantly lower than those in P group and Q group, with statistically significant differences (P < 0.05). The difference of incidence of nausea and vomiting between the three groups was not statistically significant (P > 0.05). Conclusion: Application of parecoxib sodium combined with tramadol in painless induced abortion can reduce the intraoperative consumption of propofol, and has better efficacy than simple parecoxib sodium or tramadol.

Sichuan Yixue published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C8H14O2, Name: Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Luo, Pengfei’s team published research in Zhongguo Putong Waike Zazhi in 23 | CAS: 198470-85-8

Zhongguo Putong Waike Zazhi published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C19H17N2NaO4S, Name: Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide.

Luo, Pengfei published the artcileEffects of parecoxib sodium on cognitive function of elderly patients after hepatectomy for liver cancer, Name: Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, the publication is Zhongguo Putong Waike Zazhi (2014), 23(7), 887-892, database is CAplus.

The effects of using parecoxib sodium for analgesia on post-hepatectomy cognitive function in elderly patients were investigated. Eighty patients over 60 years of age undergoing elective hepatectomy for liver cancer were randomly assigned into observational group and control group, with 40 cases in each group. Patients in observational group received parecoxib sodium administration after surgery (40 mg, i.v. injection, and once per 12 h for 3 d), and those in control group were given normal saline as placebo. And addnl. tramadol was used in either group according to need for analgesia to maintain the pain visual analog scale (VAS) not more than a score of 3. The Wechsler Adult Intelligence Scale (WAIS) and Wechsler Memory Scale (WMS) were used to test the incidence of postoperative cognitive dysfunction (POCD) in both groups of patients, and the blood levels of S-100β protein, inflammatory cytokines, cortisol, and ammonia were detected before surgery and on several time points after surgery. The perioperative data between the two groups of patients showed no statistical difference. The incidence of POCD was significantly lower in observational group than that in control group (7.5% vs. 2.5%, P<0.05). The levels of cortisol, interleukin-4 (IL-4) and ammonia had no significant alteration in both group at any postoperative time points compared with their preoperative levels. The levels of S-100β protein, IL-6, tumor necrosis factor-α (TNF-α), IL-1β and C-reactive protein (CRP) in both groups were significantly increased in different time spans with varying degrees in both groups compared with their preoperative levels, but the increasing degrees of S-100β protein and IL-6 in observational group were less than those in control group within postoperative 24 and 48 h, resp. Parecoxib sodium administration could help improve the post-hepatectomy cognitive function in elderly patients, and the mechanism might probably associated with its decreasing the S-100β and IL-6 levels.

Zhongguo Putong Waike Zazhi published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C19H17N2NaO4S, Name: Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Sibi, Mukund P.’s team published research in Journal of Organic Chemistry in 62 | CAS: 182122-10-7

Journal of Organic Chemistry published new progress about 182122-10-7. 182122-10-7 belongs to isoxazole, auxiliary class BOX or PyBox,BOX or PyBox, name is (3aS,3a’S,8aR,8a’R)-2,2′-(Cyclobutane-1,1-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole), and the molecular formula is C15H10O2, Name: (3aS,3a’S,8aR,8a’R)-2,2′-(Cyclobutane-1,1-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole).

Sibi, Mukund P. published the artcilePractical and Efficient Enantioselective Conjugate Radical Additions, Name: (3aS,3a’S,8aR,8a’R)-2,2′-(Cyclobutane-1,1-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole), the publication is Journal of Organic Chemistry (1997), 62(12), 3800-3801, database is CAplus.

Outstanding levels of enantioselectivity (up to 97% ee) using catalytic amounts of chiral Lewis acids in conjugate radical additions was achieved. Addnl., high levels of enantioselectivity at room temperature using sub-stoichiometric amounts of chiral Lewis acid are also reported. Thus, iso-Pr radical addition to N-cinnamoyl oxazolidinone at -78° using a chiral Lewis acid derived from MgI2 and chiral bioxazoline (4S,5R)-I in sub-stoichiometric yield (40 mol %) provides conjugate addition product (R)-II of high optical purity (94% isolated yield, 97% ee). The effects of bite angle and dihedral angle in a variety of chiral bioxazoline ligands on the enantioselectivity and absolute stereochem. of the conjugate radical addition reaction were studied.

Journal of Organic Chemistry published new progress about 182122-10-7. 182122-10-7 belongs to isoxazole, auxiliary class BOX or PyBox,BOX or PyBox, name is (3aS,3a’S,8aR,8a’R)-2,2′-(Cyclobutane-1,1-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole), and the molecular formula is C15H10O2, Name: (3aS,3a’S,8aR,8a’R)-2,2′-(Cyclobutane-1,1-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole).

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem