Acetal and ketal deprotection using Montmorillonite K10: The first synthesis of syn-4,8-dioxatricyclo[5.1.0.0^3,5]-2,6-octanedione

TY - JOUR

T1 - Acetal and ketal deprotection using Montmorillonite K10: The first synthesis of syn-4,8-dioxatricyclo[5.1.0.03,5]-2,6-octanedione

AU - Gautier, Elisabeth C.L.

AU - Graham, Andrew E.

AU - McKillop, Alexander

AU - Standen, Stephen P.

AU - Taylor, Richard J.K.

PY - 1997/3/17

Y1 - 1997/3/17

N2 - Montmorillonite K10 in dichloromethane at room temperature conveniently and efficiently converts acetals and ketals into the corresponding carbonyl compounds. The title dione (diepoxy-1,4- cyclohexanedione) has been prepared for the brat lime using this procedure.

AB - Montmorillonite K10 in dichloromethane at room temperature conveniently and efficiently converts acetals and ketals into the corresponding carbonyl compounds. The title dione (diepoxy-1,4- cyclohexanedione) has been prepared for the brat lime using this procedure.

UR - http://www.scopus.com/inward/record.url?scp=0031575828&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(97)00226-8

DO - 10.1016/S0040-4039(97)00226-8

M3 - Article

AN - SCOPUS:0031575828

SN - 0040-4039

VL - 38

SP - 1881

EP - 1884

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 11

ER -