Tetrahedron

Synthesis and reactivity of formyl-substituted photochromic 3, 3-diphenyl-[3H]-naphtho [2, 1-b] pyrans

…, V Lokshin, V Rossollin, A Samat, R Guglielmetti

Index: Chamontin, Karine; Lokshin, Vladimir; Rossollin, Valerie; Samat, Andre; Guglielmetti, Robert Tetrahedron, 1999 , vol. 55, # 18 p. 5821 - 5830

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Citation Number: 28

Abstract

Synthetic accesses to formylated photochromic 3, 3-diphenyl-[3H]-naphthopyrans (or 2H- benzochromenes) are developed through classical cyclization between appropriate hydroxynaphthaldehydes and 1, 1-diphenylpropyne-1-ol and also via substituent transformations on the naphthopyran skeleton including bromine/lithium exchange and the oxidation of an hydroxymethyl group. Examples of formyl group reactivity (Wittig and ...

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