Asymmetric synthesis of (1R, 2S, 3R)-2-acetyl-4(5)-(1,2,3,4-tetrahydroxybutyl)imidazole

Citation

• Cliff, M. D., & Pyne, S. G. (1995). Asymmetric synthesis of (1R, 2S, 3R)-2-acetyl-4(5)-(1,2,3,4-tetrahydroxybutyl)imidazole. Tetrahedron Letters, 36(33), 5969-5972. doi:10.1016/00404-0399(50)1155B-

Digital Object Identifier (doi)

• 10.1016/00404-0399(50)1155B-

Scopus Eid

• 2-s2.0-85047671332

Web Of Science Accession Number

Start Page

• 5969

End Page

• 5972

Volume

• 36

Issue

• 33

Abstract

• A method for preparing the biologically active compound (1R, 2S, 3R)-2-acetyl-4(5)-(1,2,3,4-tetrahydroxybutyl)imidazole1 using a palladium (0) catalysed coupling of 1-ethoxymethyl-4-iodoimidazole 2 to the functionalised vinylstannane 3 and the Sharpless catalytic asymmetric dihydroxylation is reported. © 1995.

UOW Authors

•   Pyne, Stephen

Publication Date

• 1995

Publisher

• Elsevier BV 

Published In

• Tetrahedron Letters  Journal

Citation

• Cliff, M. D., & Pyne, S. G. (1995). Asymmetric synthesis of (1R, 2S, 3R)-2-acetyl-4(5)-(1,2,3,4-tetrahydroxybutyl)imidazole. Tetrahedron Letters, 36(33), 5969-5972. doi:10.1016/00404-0399(50)1155B-

Digital Object Identifier (doi)

• 10.1016/00404-0399(50)1155B-

Scopus Eid

• 2-s2.0-85047671332

Web Of Science Accession Number

Start Page

• 5969

End Page

• 5972

Volume

• 36

Issue

• 33