The Journal of Organic Chemistry

Synthesis of. alpha.-halocinnamate esters via solvolytic rearrangement of trichloroallyl alcohols

WJ Kruper Jr, AH Emmons

Index: Journal of Organic Chemistry, , vol. 56, # 10 p. 3323 - 3329

Full Text: HTML

Citation Number: 24

Abstract

... conditions, the resulting esters were frequently found to be pure enough to conduct subsequent Michael chemistry without complication. ... All preparative chro- matography of organic compounds was performed with use of the flash chromatography (Merck Grade 60,23(MOo ... J. Org ...

Related Articles:

Preparation of α-haloacrylate derivatives via dimethyl sulfoxide-mediated selective dehydrohalogenation

[Organic Letters, , vol. 9, # 22 p. 4607 - 4610]

Stereoselective dehydrobromination of alkyl α-Brα-Cl-carboxylates

[Tetrahedron Letters, , vol. 36, # 17 p. 3023 - 3026]

Effect of a carbonyl group on the ring opening of a neighboring bromonium ion

[Journal of Organic Chemistry, , vol. 44, p. 2608 - 2611]

Zinc promoted addition of methyl 2, 2-dihalocarboxylates to carbonyl compounds

[Synthetic Communications, , vol. 26, # 22 p. 4113 - 4122]

Selenium in synthesis. Conjugated vinylic ethers, esters, and halides from. alpha.-hetero-substituted selenides

[Journal of Organic Chemistry, , vol. 43, # 8 p. 1607 - 1608]

More Articles...