Synthetic communications

Dibromomethane as One??Carbon Source in Organic Synthesis: Formal Total Synthesis of (±)??Nephrosteranic Acid

YS Hon, CH Hsieh, HF Chen

Index: Hon, Yung-Son; Hsieh, Cheng-Han; Chen, Hsien-Fan Synthetic Communications, 2007 , vol. 37, # 10 p. 1635 - 1651

Full Text: HTML

Citation Number: 7

Abstract

Abstract A diastereoselective formal total synthesis of (±)??nephrosteranic acid (10) is described. The key step is to introduce the α??methylene group by the ozonolysis of monosubstituted alkenes followed by reaction with a preheated mixture of CH2Br2–Et2NH. The α??methyl group of compound 10 was formed from the reduction of the corresponding α?? methylene precursor.

Related Articles:

Enantioselective synthesis of α-amino acids from n-tosyloxy β-lactams derived from β-keto esters

[Journal of Organic Chemistry, , vol. 68, # 1 p. 27 - 34]

Enantioselective synthesis of α-amino acids from n-tosyloxy β-lactams derived from β-keto esters

[Journal of Organic Chemistry, , vol. 68, # 1 p. 27 - 34]

Gas chromatography/electron-capture negative ion mass spectrometry for the quantitative determination of 2-and 3-hydroxy fatty acids in bovine milk fat

[Journal of Agricultural and Food Chemistry, , vol. 56, # 14 p. 5500 - 5505]

New potential immunoenhancing compounds. Synthesis and pharmacological evaluation of new long-chain 2-amido-2-deoxy-D-glucose derivatives.

[Arzneimittel-Forschung/Drug Research, , vol. 39, # 10 p. 1190 - 1195]

New potential immunoenhancing compounds. Synthesis and pharmacological evaluation of new long-chain 2-amido-2-deoxy-D-glucose derivatives.

[Arzneimittel-Forschung/Drug Research, , vol. 39, # 10 p. 1190 - 1195]

More Articles...