Production Method 1

110994-91-7

82079-45-6

Reaction Conditions

1.1 Reagents: Potassium hydroxide Solvents: Ethanol ;  1.5 h, -20 °C; -20 °C → 0 °C; 17 h, 0 °C
1.2 Solvents: Ethanol ,  Water ;  30 min, rt → reflux

Reference

Total Synthesis of Solandelactone I

Eichenauer, Nils C.; et al, Journal of Natural Products, 2015, 78(11), 2782-2790

Production Method 2

118712-39-3

82079-45-6

Reaction Conditions

1.1 Reagents: Potassium hydroxide Solvents: Ethanol ,  Water ;  1 h, 60 °C

Reference

Total synthesis of violaceimides A-E and consideration of the reported stereochemistry

Perry, Charles K.; et al, Tetrahedron Letters, 2019, 60(40),

Production Method 3

312-84-5

82079-45-6

Reaction Conditions

1.1 Reagents: Sodium nitrite ,  Potassium bromide ,  Hydrogen bromide Solvents: Water
1.2 Reagents: Potassium methoxide Solvents: Methanol

Reference

Preparation of enantiomerically pure α-hydroxy esters and α-hydroxy aldehydes. Application to the enantiospecific synthesis of the sex pheromone of the mealybug Pseudococcus comstocki

Larcheveque, Marc; et al, Bulletin de la Societe Chimique de France, 1989, (1), 130-9

Production Method 4

110994-91-7

82079-45-6

Reaction Conditions

Reference

Optically active epoxides as drug and agrochemical intermediate and their preparation

, France, , ,

Production Method 5

110994-91-7

82079-45-6

Reaction Conditions

1.1 Reagents: Potassium hydroxide Solvents: Ethanol

Reference

A simple preparation of R- or S-glycidic esters; application to the synthesis of enantiomerically pure α-hydroxy esters

Larcheveque, Marc; et al, Tetrahedron Letters, 1987, 28(18), 1993-6

Production Method 6

312-84-5

82079-45-6

Reaction Conditions

1.1 Reagents: Sodium nitrite ,  Potassium bromide ,  Hydrogen bromide Solvents: Water ;  1 h, 20 psi, < 5 °C
1.2 Reagents: Potassium hydroxide Solvents: Ethanol ;  0 °C → 20 °C; 1 h, -5 - 5 °C

Reference

Practical Asymmetric Synthesis of an Edivoxetine·HCl Intermediate via an Efficient Diazotization Process

Kopach, Michael E.; et al, Organic Process Research & Development, 2015, 19(4), 543-550

Potassium (S)-oxirane-2-carboxylate Raw materials

• D-Serine
• methyl (2S)-oxirane-2-carboxylate
• Propanoic acid, 2-bromo-3-hydroxy-, (R)-

Potassium (S)-oxirane-2-carboxylate Preparation Products

• Potassium (S)-oxirane-2-carboxylate (82079-45-6)

• 1. Emulsifier-free, organotellurium-mediated living radical emulsion polymerization (emulsion TERP) of styrene: poly(dimethylaminoethyl methacrylate) macro-TERP agent?
  Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
• 2. Estimation of activation energy for electroporation and pore growth rate in liquid crystalline and gel phases of lipid bilayers using molecular dynamics simulations?
  Amit Kumar Majhi,Subbarao Kanchi,V. Venkataraman,K. G. Ayappa,Prabal K. Maiti Soft Matter, 2015,11, 8632-8640
• 3. Excellent mechanical performance and enhanced dielectric properties of OBC/SiO2 elastomeric nanocomposites: effect of dispersion of the SiO2 nanoparticles?
  Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
• 4. Dissolution of cork biopolymers in biocompatible ionic liquids
  Helga Garcia,Rui Ferreira,Marija Petkovic,Jamie L. Ferguson,Maria C. Leit?o,H. Q. Nimal Gunaratne,Luís Paulo N. Rebelo Green Chem., 2010,12, 367-369
• 5. Esterase-responsive polymeric prodrug-based tumor targeting nanoparticles for improved anti-tumor performance against colon cancer?
  Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun Cao RSC Adv., 2016,6, 42109-42119

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Epoxides Oxirane carboxylic acids
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Epoxides Oxirane carboxylic acids and derivatives Oxirane carboxylic acids

• 111058-32-3(methyl (2R)-oxirane-2-carboxylate)
• 4538-50-5(methyl oxirane-2-carboxylate)
• 51877-54-4(oxirane-2-carboxylic acid;potassium salt)
• 23943-96-6((2R)-2-methoxypropanoic acid)
• 26023-30-3(Poly[oxy(1-methyl-2-oxo-1,2-ethanediyl)])
• 23953-00-6((2S)-2-methoxypropanoic acid)
• 118712-39-3(methyl (2S)-oxirane-2-carboxylate)
• 6311-64-4(2,3-Oxiranedicarboxylicacid, potassium salt (1:2))
• 503-11-7(oxirane-2-carboxylic acid)
• 55203-13-9(Propanedioic acid, 2,2'-oxybis-)