Synthesis, chemistry, and absolute configuration of novel transglutaminase inhibitors containing a 3-halo-4,5-dihydroisoxazole
- 1 September 1988
- journal article
- Published by Elsevier in Bioorganic Chemistry
- Vol. 16 (3) , 335-340
- https://doi.org/10.1016/0045-2068(88)90019-3
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Tetrahydrofurans via isoxazoline: a tandem 1,3-dipolar cycloaddition/electrophilic cyclization sequenceJournal of the American Chemical Society, 1987
- Sulfonylisoxazolines: reliable intermediates for the preparation of .beta.-hydroxy nitrilesThe Journal of Organic Chemistry, 1987
- An easy synthesis of dihydromuscimolTetrahedron Letters, 1986
- Precocious appearance of involucrin and epidermal transglutaminase during differentiation of psoriatic skinBritish Journal of Dermatology, 1986
- Acivicin in 1985Advances in Enzyme Regulation, 1985
- GABA agonists. Resolution, absolute stereochemistry and enantioselectivity of (S)-(+)- and (R)-(-)-dihydromuscimolJournal of Medicinal Chemistry, 1985
- Reduction of substituted .DELTA.2-isoxazolines. Synthesis of .beta.-hydroxy acid derivativesThe Journal of Organic Chemistry, 1984
- Transglutaminase Activity in Human and Rabbit Ear Comedogenesis: A Histochemical StudyJournal of Investigative Dermatology, 1984
- Cyanogen chloride N-oxide cycloadditions. A simple, short route to AT-125.Tetrahedron Letters, 1982
- Total synthesis of .alpha.-amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid (AT-125), an antitumor antibioticJournal of the American Chemical Society, 1979