Formal [4+2] cycloaddition of di-tert-butyl 2-ethoxycyclobutane-1,1-dicarboxylate with ketones or aldehydes and tandem lactonization.

Abstract:

:A catalytic amount of tin(IV) chloride catalyzed formal [4+2] cycloaddition reaction of di-tert-butyl 2-ethoxycyclobutane-1,1-carboxylate with ketones or aldehydes to give diethyl 6-ethoxydihydro-2H-pyran-3,3(4H)-dicarboxylates, whereas two equivalents of trimethylsilyl triflate promoted tandem [4+2] cycloaddition and lactonization to afford 3-oxo-2,6-dioxabicyclo[2.2.2]octane-4-carboxylate esters.

authors

Okado R,Nowaki A,Matsuo J,Ishibashi H

doi

10.1248/cpb.60.21

subject

Has Abstract

pub_date

2012-01-01 00:00:00

pages

21-2

issue

1

eissn

0009-2363

issn

1347-5223

pii

JST.JSTAGE/cpb/60.21

journal_volume

60

pub_type

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