跳转至内容
Merck
CN
  • Formal [4+2] cycloaddition of di-tert-butyl 2-ethoxycyclobutane-1,1-dicarboxylate with ketones or aldehydes and tandem lactonization.

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

Chemical & pharmaceutical bulletin (2012-01-10)
Ryohei Okado, Aya Nowaki, Jun-Ichi Matsuo, Hiroyuki Ishibashi
摘要

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.

材料
产品编号
品牌
产品描述

Sigma-Aldrich
氯化锡(II), reagent grade, 98%
Sigma-Aldrich
氯化锡(II) 二水合物, ACS reagent, 98%
Sigma-Aldrich
氯化锡(II) 二水合物, reagent grade, 98%
Sigma-Aldrich
氯化锡(II) 二水合物, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥98%
Sigma-Aldrich
氯化锡(II) 二水合物, ≥99.99% trace metals basis
Sigma-Aldrich
氯化锡(II) 二水合物, ≥99.97% trace metals basis
Sigma-Aldrich
氯化锡(II), anhydrous, powder, ≥99.99% trace metals basis
Sigma-Aldrich
氯化锡(II), ≥99.99% trace metals basis
Supelco
氯化锡(II) 二水合物, suitable for AAS