Jill Gigg

The allyl ether as a protecting group in carbohydrate chemistry

Jill Gigg, Roy Gigg · Journal of the Chemical Society C Organic · 1966 · 93 citations

Deep Eutectic Solvent, Bioorganic Chemistry, Prop-1-enyl Group +12

(±)-1,2:4,5-Di-O-isopropylidene-myo-inositol

Jill Gigg, Roy Gigg, Sheila Payne et al. · Carbohydrate Research · 1985 · 82 citations

The allyl group for protection in carbohydrate chemistry. Part 21. (±)-1,2 : 5.6- and (±)-1,2 : 3,4-di-O-isopropylidene-myo-inositol. The unusual behaviour of crystals of (±)-3,4-di-O-acetyl-1,2,5,6-tetra-O-benzyl-myo-inositol on heating and cooling: a ‘thermosalient solid’

Jill Gigg, Roy Gigg, Sheila Payne et al. · Journal of the Chemical Society Perkin Transactions 1 · 1987 · 70 citations

The allyl group for protection in carbohydrate chemistry. Part 18. Allyl and benzyl ethers of myo-inositol. Intermediates for the synthesis of myo-inositol trisphosphates

Jill Gigg, Roy Gigg, Sheila Payne et al. · Journal of the Chemical Society Perkin Transactions 1 · 1987 · 67 citations

Diversity Oriented Synthesis, Bioorganic Chemistry, Engineering +12

Use of synthetic glycoconjugates containing the Mycobacterium leprae specific and immunodominant epitope of phenolic glycolipid I in the serology of leprosy.

Sara Brett, Sheila Payne, Jill Gigg et al. · PubMed · 1986 · 63 citations · Full text

Mycobacterium Leprae Specific, Immunology, Glycobiology +16