ACID-MEDIATED CYCLIZATIONS - EFFICIENT ACCESS TO FUNCTIONALIZED TRANS-DECALINS

Authors
LINDER SM REICHLIN D SIMMONS DP SNOWDEN RL
Citation
Sm. Linder et al., ACID-MEDIATED CYCLIZATIONS - EFFICIENT ACCESS TO FUNCTIONALIZED TRANS-DECALINS, Tetrahedron letters, 34(30), 1993, pp. 4789-4792
Citations number
9
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
30
Year of publication
1993
Pages
4789 - 4792
Database
ISI
SICI code
0040-4039(1993)34:30<4789:AC-EAT>2.0.ZU;2-R
Abstract
Acid-mediated cyclisation of monocyclic, (E)- and (Z)-beta-phosphoroxy enoate 5d using 98% aq. H2SO4 in toluene at 2-degrees affords, after d ecarbomethoxylation, trans-2-decalone 1 in 79% and 68% yield, respecti vely.