Total synthesis of acetylmelodorinol

S Chien-Chang, C Shiu-Ching, C Cheng-Jen…

Index: Shen, Chien-Chang; Chou, Shiu-Ching; Chou, Cheng-Jen; Ho, Li-Kang Tetrahedron Asymmetry, 1996 , vol. 7, # 11 p. 3141 - 3146

Full Text: HTML

Citation Number: 16

Abstract

An enantioselective total synthesis of bioactive melodorinol and acetylmelodorinol starting from 2, 3-O-isopropylidene-d-glyceraldehyde and an alkoxyfuran is reported. Lithiation of the alkoxyfuran and subsequent reaction with the glyceraldehyde provided two diastereomers. These two adducts were treated with p-toluenesulfonic acid in aqueous THF to give a γ-propylidene butenolide, which was converted to melodorinol and ...

Related Articles:

Total synthesis of both enantiomers of melodorinol. Redetermination of their absolute configurations

[Lu, Xiyan; Chen, Guoying; Xia, Lijun; Guo, Guangzhong Tetrahedron Asymmetry, 1997 , vol. 8, # 18 p. 3067 - 3072]

Total synthesis of (S)-(+)-melodorinol and (S)-(+)-acetylmelodorinol

[Pohmakotr, Manat; Tuchinda, Patoomratana; Premkaisorn, Pornchai; Limpongpan, Attasit; Reutrakul, Vichai Heterocycles, 1999 , vol. 51, # 4 p. 795 - 802]

More Articles...