𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of Regioselectively Deuterated Cyclopropanes

✍ Scribed by Duffault, Jean-Marc; Hanoteau, Pascal; Parrilla, Alfredo; Einhorn, Jacques

Book ID
120326180
Publisher
Taylor and Francis Group
Year
1996
Tongue
English
Weight
366 KB
Volume
26
Category
Article
ISSN
0039-7911

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Regioselective synthesis of deuterated a
Regioselective synthesis of deuterated analogs of the neurotoxin MPTP
✍ StΓ©phane Mabic; Neal Castagnoli Jr. πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 French βš– 312 KB πŸ‘ 1 views

1 -Methyl-4-phenyl-2-pyridone has been used as starting material for the efficient and regioselective synthesis of deuterated analogues of the neurotoxin 1 -methyl-4-phenyl-l,2,3,6-tetrahydropyridine (MPTP). MPTP-2,242, MPTP-6,6-& and MPTP-2,2,6,6-d4 were obtained in good yield through a combination

Regioselective cyclopropanation reaction
Regioselective cyclopropanation reactions using iodonium ylides: Synthesis of prostaglandin precursors
✍ Robert M. Moriarty; Eric J. May; Liang Guo; Om Prakash πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 119 KB

Iodonium ylides of methyl 3-oxo-trans,trans-6,8-tetradecadienoate (1) and diprotected methyl 3,5-di(tbutyldimethyl-silyloxy)-2,6,8-tetradecalrieneoate (5) undergo regio-and stereoselective inwamolecular cyclopropanation with Cu(I)CI catalysis to form key bicyclo[3.1.0] intermediates for prostaglandi