Convenient access to meso benzylic bis-alkynes

Philip Bulman Page; Richard Stephenson; James Harvey; Annie-Claude Gaumont; Carole Alayrac; Alexandra Slawin

doi:10.1055/s-0035-1561318

Convenient access to meso benzylic bis-alkynes

Philip Bulman Page
, Richard Stephenson
, James Harvey
, Annie-Claude Gaumont
, Carole Alayrac
, Alexandra Slawin

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

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Abstract

meso bis-Alkynes and alkenes have potential as substrates for desymmetrization processes. The preparation of several meso bis(1’-hydroxy-2’-propynyl)benzenes and their derivatives from phthalaldehydes using inexpensive and readily available reagents is described

Original language	English
Pages (from-to)	961-964
Number of pages	4
Journal	Synlett
Volume	27
Issue number	06
Early online date	11 Jan 2016
DOIs	https://doi.org/10.1055/s-0035-1561318
Publication status	Published - 11 Jan 2016

Keywords

meso
desymmetrization
bisalkyne
phthalaldehyde

Access to Document

10.1055/s-0035-1561318

meso diyne declicked 6-12-15 SLAccepted author manuscript, 967 KB

Cite this

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title = "Convenient access to meso benzylic bis-alkynes",

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AU - Bulman Page, Philip

AU - Stephenson, Richard

AU - Harvey, James

AU - Gaumont, Annie-Claude

AU - Alayrac, Carole

AU - Slawin, Alexandra

PY - 2016/1/11

Y1 - 2016/1/11

N2 - meso bis-Alkynes and alkenes have potential as substrates for desymmetrization processes. The preparation of several meso bis(1’-hydroxy-2’-propynyl)benzenes and their derivatives from phthalaldehydes using inexpensive and readily available reagents is described

AB - meso bis-Alkynes and alkenes have potential as substrates for desymmetrization processes. The preparation of several meso bis(1’-hydroxy-2’-propynyl)benzenes and their derivatives from phthalaldehydes using inexpensive and readily available reagents is described

KW - meso

KW - desymmetrization

KW - bisalkyne

KW - phthalaldehyde

U2 - 10.1055/s-0035-1561318

DO - 10.1055/s-0035-1561318

M3 - Article

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VL - 27

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JF - Synlett

IS - 06

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