Literature DB >> 12167042

A nonspectroscopic method to determine the photolytic decomposition pathways of 3-chloro-3-alkyldiazirine: carbene, diazo and rearrangement in excited state.

Takatsugu Wakahara1, Yasuyuki Niino, Takashi Kato, Yutaka Maeda, Takeshi Akasaka, Michael T H Liu, K Kobayashi, S Nagase.   

Abstract

C(60) acts as a mechanistic probe for the formation of carbene, diazo compound, and for the rearranged product via the excited state in the photolysis of 3-chloro-3-isopropyldiazirine and 3-chloro-3-chloromethyldiazirine. The carbene adds to C(60) to form methanofullerene, whereas the diazo compound adds to C(60) to form fulleroid. The olefin product arises as a result of the rearrangement in the excited state.

Entities:  

Year:  2002        PMID: 12167042     DOI: 10.1021/ja0116876

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

Review 1.  Current advances of carbene-mediated photoaffinity labeling in medicinal chemistry.

Authors:  Sha-Sha Ge; Biao Chen; Yuan-Yuan Wu; Qing-Su Long; Yong-Liang Zhao; Pei-Yi Wang; Song Yang
Journal:  RSC Adv       Date:  2018-08-20       Impact factor: 4.036

2.  3-Trifluoromethyl-3-aryldiazirine photolabels with enhanced ambient light stability.

Authors:  Arun Babu Kumar; Jeremiah D Tipton; Roman Manetsch
Journal:  Chem Commun (Camb)       Date:  2016-02-14       Impact factor: 6.065

  2 in total

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