NEW SYNTHESIS OF PHENYLACETAMIDES AND DIHYDROPYRAZINS VIA ISOCYANIDE-BASED SEQUENTIAL UGI/STAUDINGER/INTRAMOLECULAR NUCLEOPHILIC CYCLIZATION

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AMANPOUR TAYEBEH; BAZGIR AYOOB

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Seminar Paper

Paper Information

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

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Title

NEW SYNTHESIS OF PHENYLACETAMIDES AND DIHYDROPYRAZINS VIA ISOCYANIDE-BASED SEQUENTIAL UGI/STAUDINGER/INTRAMOLECULAR NUCLEOPHILIC CYCLIZATION

Author(s)

AMANPOUR TAYEBEH | BAZGIR AYOOB | Issue Writer Certificate

Keywords

ISOCYANIDE

STAUDINGER REACTION

UGI REACTION

Abstract

THE AZA-WITTIG REACTIONS OF IMINOPHOSPHORANES HAVE RECEIVED INCREASED ATTENTION IN VIEW OF THEIR UTILITY IN THE SYNTHESIS OF N -HETEROCYCLES [1]. RECENTLY THE SEQUENCE OF UGI AND PASSERINI REACTION, FOLLOWED BY POST-CONDENSATION STAUDINGER AND AZA-WITTIG REACTION, HAS BEEN UTILIZED IN SYNTHESIS OF A SERIES OF BIOLOGICALLY USEFUL HETEROCYCLES [2]. CONTINUING OUR INTEREST IN THE SYNTHESIS OF VARIOUS HETEROCYCLES VIA AZA-WITTIG REACTION [3], WE WISH TO REPORT HEREIN A ONE-POT SYNTHETIC APPROACH TO PHENYLACETAMIDES AND DIHYDROPYRAZINSBY A SEQUENTIAL UGI4CC-STAUDINGEREAZA-WITTIG REACTION.

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APA: Copy

BAZGIR, AYOOB. (2014). NEW SYNTHESIS OF PHENYLACETAMIDES AND DIHYDROPYRAZINS VIA ISOCYANIDE-BASED SEQUENTIAL UGI/STAUDINGER/INTRAMOLECULAR NUCLEOPHILIC CYCLIZATION. IRANIAN SEMINAR OF ORGANIC CHEMISTRY. SID. https://sid.ir/paper/913991/en

Vancouver: Copy

BAZGIR AYOOB. NEW SYNTHESIS OF PHENYLACETAMIDES AND DIHYDROPYRAZINS VIA ISOCYANIDE-BASED SEQUENTIAL UGI/STAUDINGER/INTRAMOLECULAR NUCLEOPHILIC CYCLIZATION. 2014. Available from: https://sid.ir/paper/913991/en

IEEE: Copy

AYOOB BAZGIR, “NEW SYNTHESIS OF PHENYLACETAMIDES AND DIHYDROPYRAZINS VIA ISOCYANIDE-BASED SEQUENTIAL UGI/STAUDINGER/INTRAMOLECULAR NUCLEOPHILIC CYCLIZATION,” presented at the IRANIAN SEMINAR OF ORGANIC CHEMISTRY. 2014, [Online]. Available: https://sid.ir/paper/913991/en

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