Regioselective synthesis of beta-iodo-enamides and beta-yn-enamides

A E Pasqua; Lynne H Thomas; J J Crawford; R Marquez

doi:10.1016/j.tet.2011.07.033

Regioselective synthesis of beta-iodo-enamides and beta-yn-enamides

A E Pasqua, Lynne H Thomas, J J Crawford, R Marquez

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

14 Citations (SciVal)

Abstract

Iodo-enamides were synthesised in a single step, in good yield and with complete selectivity from N-formyl imides. The beta-iodo-enamides are stable and were converted efficiently into novel geometrically defined beta-yn-enamides.

Original language	English
Pages (from-to)	7611-7617
Number of pages	7
Journal	Tetrahedron
Volume	67
Issue number	39
DOIs	https://doi.org/10.1016/j.tet.2011.07.033
Publication status	Published - 30 Sept 2011

Keywords

yn-enamides
takai
halo-enamides
enamides

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10.1016/j.tet.2011.07.033

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@article{fd727d33aa334c6cab435b18df39b425,

title = "Regioselective synthesis of beta-iodo-enamides and beta-yn-enamides",

abstract = "Iodo-enamides were synthesised in a single step, in good yield and with complete selectivity from N-formyl imides. The beta-iodo-enamides are stable and were converted efficiently into novel geometrically defined beta-yn-enamides.",

keywords = "yn-enamides, takai, halo-enamides, enamides",

author = "Pasqua, {A E} and Thomas, {Lynne H} and Crawford, {J J} and R Marquez",

year = "2011",

month = sep,

day = "30",

doi = "10.1016/j.tet.2011.07.033",

language = "English",

volume = "67",

pages = "7611--7617",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier",

number = "39",

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TY - JOUR

T1 - Regioselective synthesis of beta-iodo-enamides and beta-yn-enamides

AU - Pasqua, A E

AU - Thomas, Lynne H

AU - Crawford, J J

AU - Marquez, R

PY - 2011/9/30

Y1 - 2011/9/30

N2 - Iodo-enamides were synthesised in a single step, in good yield and with complete selectivity from N-formyl imides. The beta-iodo-enamides are stable and were converted efficiently into novel geometrically defined beta-yn-enamides.

AB - Iodo-enamides were synthesised in a single step, in good yield and with complete selectivity from N-formyl imides. The beta-iodo-enamides are stable and were converted efficiently into novel geometrically defined beta-yn-enamides.

KW - yn-enamides

KW - takai

KW - halo-enamides

KW - enamides

UR - http://www.scopus.com/inward/record.url?scp=80052036369&partnerID=8YFLogxK

UR - http://dx.doi.org/10.1016/j.tet.2011.07.033

U2 - 10.1016/j.tet.2011.07.033

DO - 10.1016/j.tet.2011.07.033

M3 - Article

SN - 0040-4020

VL - 67

SP - 7611

EP - 7617

JO - Tetrahedron

JF - Tetrahedron

IS - 39

ER -

Regioselective synthesis of beta-iodo-enamides and beta-yn-enamides

Abstract

Keywords

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Raman confocal microscope RENISHAM INVIA

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Regioselective synthesis of beta-iodo-enamides and beta-yn-enamides

Abstract

Keywords

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Equipment

Raman confocal microscope RENISHAM INVIA

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