Production Method 1

946152-71-2

946152-72-3

Reaction Conditions

1.1 Reagents: Lithium hydroxide Solvents: Tetrahydrofuran ,  Water ;  overnight, rt; rt → 55 °C; 24 h, 55 °C
1.2 Solvents: Methanol ,  Tetrahydrofuran ;  3 h, 55 °C

Reference

Preparation of substituted azabicycloheptanes as orexin-1 and orexin-2 receptor antagonists

, United Kingdom, , ,

Production Method 2

946152-72-3

Reaction Conditions

Reference

Novel steroid payloads, steroid linkers, ADCs containing and use thereof

, World Intellectual Property Organization, , ,

Production Method 3

946152-71-2

946152-72-3

Reaction Conditions

1.1 Reagents: Lithium hydroxide Solvents: Tetrahydrofuran ,  Water ;  overnight, rt
1.2 Reagents: Potassium bisulfate Solvents: Water ;  acidified

Reference

Preparation of 3,7-diazabicyclo[3.3.0]octane compounds as antiviral agents

, World Intellectual Property Organization, , ,

Production Method 4

946152-71-2

946152-72-3

Reaction Conditions

1.1 Reagents: Lithium hydroxide Solvents: Tetrahydrofuran ,  Water ;  overnight, rt

Reference

pyrrolo[3,4-c]pyrrole derivatives as heterocyclic antiviral compounds and CCR5 receptor antagonists and their preparation, pharmaceutical compositions and use in the treatment of HIV infection, AIDS and ARC

, United States, , ,

Production Method 5

946152-71-2

946152-72-3

Reaction Conditions

1.1 Reagents: Lithium hydroxide Solvents: Tetrahydrofuran ,  Water ;  overnight, rt; rt → 55 °C; 24 h, 55 °C
1.2 Solvents: Methanol ,  Tetrahydrofuran ;  3 h, 55 °C

Reference

Substituted 2-azabicyclo[3.1.1]heptane and 2-azabicyclo[3.2.1]octane derivatives as orexin receptor antagonists

, World Intellectual Property Organization, , ,

3-(tert-butoxycarbonylamino)cyclobutanecarboxylic acid Raw materials

• ethyl 3-[(tert-butoxycarbonyl)amino]cyclobutanecarboxylate

3-(tert-butoxycarbonylamino)cyclobutanecarboxylic acid Preparation Products

• 3-(tert-butoxycarbonylamino)cyclobutanecarboxylic acid (946152-72-3)

• 1. An amorphous Cu–In–S nanoparticle-based precursor ink with improved atom economy for CuInSe2 solar cells with 10.85% efficiency?
  Green Chem., 2017,19, 1268-1277
• 2. Acetyl group orientation modulates the electronic ground-state asymmetry of the special pair in purple bacterial reaction centers
  P. K. Wawrzyniak,M. T. P. Beerepoot,H. J. M. de Groot,F. Buda Phys. Chem. Chem. Phys., 2011,13, 10270-10279
• 3. An atmosphere and light tuned highly diastereoselective synthesis of cyclobuta/penta[b]indoles from aniline-tethered alkylidenecyclopropanes with alkynes?
  Bo Cao,Yin Wei Chem. Commun., 2018,54, 2870-2873
• 4. An arsenic trioxide nanoparticle prodrug (ATONP) potentiates a therapeutic effect on an aggressive hepatocellular carcinoma model via enhancement of intratumoral arsenic accumulation and disturbance of the tumor microenvironment?
  Xin Fu,Qing-rong Liang,Rong-guang Luo,Yan-shu Li,Xiao-ping Xiao,Lu-lu Yu,Wen-zhe Shan,Guang-qin Fan J. Mater. Chem. B, 2019,7, 3088-3099
• 5. Alternative donor substrates for inverting and retaining glycosyltransferases?
  Luke L. Lairson,Warren W. Wakarchuk Chem. Commun., 2007, 365-367

• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Amino acids and derivatives

• 53292-90-3(cis-4-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid)
• 334932-13-7(3-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid)
• 939400-34-7(trans-3-(Tert-butoxycarbonylamino)cyclobutanecarboxylic acid)
• 53292-89-0(trans-4-(tert-Butoxycarbonylamino)cyclohexanecarboxylic Acid)
• 130309-46-5(4-(tert-butoxy)carbonylcyclohexane-1-carboxylic acid)
• 222530-33-8(cis-(+/-)-3-(Boc-amino)cyclohexanecarboxylic Acid)
• 222530-34-9((1S,3R)-3-(Tert-Butoxycarbonylamino)cyclohexanecarboxylic Acid)
• 218772-92-0(trans-3-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid)
• 222530-39-4((1R,3S)-3-(Tert-Butoxycarbonylamino)cyclohexanecarboxylic Acid)
• 1008773-79-2(cis-3-(tert-butoxycarbonylamino)cyclobutanecarboxylic acid)