1-PYRENYLMETHYL ESTERS, PHOTOLABILE PROTECTING GROUPS FOR CARBOXYLIC ACIDS

DOI: 10.1016/S0040-4039(00)95811-8

Source and publish data:

Tetrahedron Letters p. 679 - 682 (1987)

Update date:2022-08-04

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Authors:

Iwamura, Michiko

Ishikawa, Touru

Koyama, Yukiyoshi

Sakuma, Keisuke

Iwamura, Hiizu

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Article abstract of DOI:10.1016/S0040-4039(00)95811-8

1-Diazomethylpyrenes were prepared and reacted with carboxylic acids to give 1-pyrenylmethyl esters.The fluorescent esters were photolysed at 340 nm in methanol to form the starting acids and the corresponding 1-methoxymethylpyrenes in high yields.

Full text of DOI:10.1016/S0040-4039(00)95811-8

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Article Doi

1-PYRENYLMETHYL ESTERS, PHOTOLABILE PROTECTING GROUPS FOR CARBOXYLIC ACIDS

DOI: 10.1016/S0040-4039(00)95811-8

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)95811-8

Full text of DOI:10.1016/S0040-4039(00)95811-8

Products guided by the article

R&D Labs maybe for 855-25-4

Relevant to this article

Metal carbenoid mediated ring opening of furan-2-yloxy derivatives. Stereoselective synthesis of 2,4-hexadienedioic acid and 6-aryl-1-oxo-2,4-hexadienoic acid derivatives

Unexpected stability of aryl β-N-acetylneuraminides in neutral solution: Biological implications for sialyl transfer reactions

Concise syntheses of selective inhibitors against α-1,3- galactosyltransferase

Solvent selective phenyl selenylation and phenyl tellurylation of aryl boronic acids catalyzed by Cu(II) grafted functionalized polystyrene

Synthesis of 2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)-ones by the domino Michael addition retro-ene reaction of 2-alkoxyiminoimidazolidines and acetylene carboxylates

Contrasting ESR and UV Spectroscopic Properties and Reactivities between the Conformationally Restricted o-(9-Fluorenyl)phenylnitrenes at Cryogenic Temperatures