Isostere-Based Design of 8-Azacoumarin-Type Photolabile Protecting Groups: A Hydrophilicity-Increasing Strategy for Coumarin-4-ylmethyls-Reference-Cited by-同舟云学术

Isostere-Based Design of 8-Azacoumarin-Type Photolabile Protecting Groups: A Hydrophilicity-Increasing Strategy for Coumarin-4-ylmethyls

Published:2014-02-04 Issue:4 Volume:16 Page:1184-1187
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Narumi Tetsuo¹,Takano Hikaru¹,Ohashi Nami¹,Suzuki Akinobu²,Furuta Toshiaki²,Tamamura Hirokazu¹

Affiliation:

1. Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, Chiyoda-ku, Tokyo 101-0062, Japan

2. Department of Biomolecular Science, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8510, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol5000583

Reference45 articles.

1. Photoremovable Protecting Groups in Organic Synthesis

2. bBinkley, R. W.; Flechtner, T. W.InSynthetic Organic Photochemistry;Horspool, W. M., Ed.Plenum:New York, 1984; pp375–423.

3. cPillai, V. N. R.Organic Photochemistry;Padwa, A., Ed.Marcel Dekker:New York, 1987; Vol.9, pp225–323.

4. eBochet, C. G.; Blanc, A.InCRC Handbook of Organic Photochemistry and Photobiology;Griesbeck, A.; Oelgemöller, M.; Ghetti, F., Eds.CRC:Boca Raton, 2012; Vol.1, pp73–93.

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