REGIOSELECTIVE RING OPENING OF KETOAZIRIDINES WITH ISOTHIOCYANATE

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SAMIMI H.A.; KIYANI H.; MOSTAFAVI A.

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Seminar Paper

Paper Information

Seminar: IRANIAN SEMINAR OF ORGANIC CHEMISTRY
Year:2014 | Issue:22

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Title

REGIOSELECTIVE RING OPENING OF KETOAZIRIDINES WITH ISOTHIOCYANATE

Author(s)

SAMIMI H.A. | KIYANI H. | MOSTAFAVI A. | Issue Writer Certificate

Keywords

KETOAZIRIDINE

REGIOSELECTIVE

RING OPENING

Abstract

THE AZIRIDINE MOIETY REPRESENTS ONE OF THE MOST VALUABLE THREE MEMBERED RING SYSTEMS IN ORGANIC CHEMISTRY AND THE REGIOCONTROLLED RING OPENING OF C-SUBSTITUTED AZIRIDINES CONSTITUTES A POWERFUL APPROACH TOWARD THE PREPARATION OF A LARGE VARIETY OF FUNCTIONALIZED NITROGEN-CONTAINING TARGET COMPOUNDS [1]. WIDE VARIETIES OF METHODS HAVE BEEN REPORTED FOR RING OPENING OF THE AZIRIDINES, BUT THERE ARE A FEW METHODS FOR RING OPENING OF 1, 2-DIAROYL-3-ARYLAZIRIDINES [2]. IN CONTINUATION OF OUR EFFORTS IN THE DEVELOPMENT AND SYNTHESIS OF NEW COMPOUNDS FROM KETOAZIRIDINES [3–4], WE HAVE DISCOVERED A NEW AND SIMPLE ONE-POT METHOD FOR THE RING OPENING OF TRANS-1, 2-DIAROYL-3-ARYLAZIRIDINES BY A REGIO-CONTROLLED REACTION WITH ISOTHIOCYANATE.

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APA: Copy

SAMIMI, H.A., KIYANI, H., & MOSTAFAVI, A.. (2014). REGIOSELECTIVE RING OPENING OF KETOAZIRIDINES WITH ISOTHIOCYANATE. IRANIAN SEMINAR OF ORGANIC CHEMISTRY. SID. https://sid.ir/paper/912494/en

Vancouver: Copy

SAMIMI H.A., KIYANI H., MOSTAFAVI A.. REGIOSELECTIVE RING OPENING OF KETOAZIRIDINES WITH ISOTHIOCYANATE. 2014. Available from: https://sid.ir/paper/912494/en

IEEE: Copy

H.A. SAMIMI, H. KIYANI, and A. MOSTAFAVI, “REGIOSELECTIVE RING OPENING OF KETOAZIRIDINES WITH ISOTHIOCYANATE,” presented at the IRANIAN SEMINAR OF ORGANIC CHEMISTRY. 2014, [Online]. Available: https://sid.ir/paper/912494/en

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