Carbolithiation of aromatic rings: Cyclohexadienes from N-aroyl-2,2,6,6-tetramethylpiperidines

Jonathan Clayden; Yann J Y Foricher; Ho Kam Lam

doi:10.1039/B206479K

Carbolithiation of aromatic rings: Cyclohexadienes from N-aroyl-2,2,6,6-tetramethylpiperidines

Jonathan Clayden^*
, Yann J Y Foricher
, Ho Kam Lam

^*Corresponding author for this work

School of Chemistry

Research output: Contribution to journal › Article (Academic Journal) › peer-review

17 Citations (Scopus)

Abstract

Benzamides whose nitrogen atom is part of a 2,2,6,6-tetramethylpiperidine ring are dearomatised by alkyllithiums, which attack them regioselectively to yield, after electrophilic quench, substituted cyclohexadienes.

Original language	English
Pages (from-to)	2138-2139
Number of pages	2
Journal	Chemical Communications
Issue number	18
DOIs	https://doi.org/10.1039/B206479K
Publication status	Published - 22 Aug 2002

Research Groups and Themes

Organic & Biological

Access to Document

10.1039/B206479K

Handle.net

Persistent link

Cite this

@article{87a8da38d4ce4fe18d61f81f4fb14636,

title = "Carbolithiation of aromatic rings: Cyclohexadienes from N-aroyl-2,2,6,6-tetramethylpiperidines",

abstract = "Benzamides whose nitrogen atom is part of a 2,2,6,6-tetramethylpiperidine ring are dearomatised by alkyllithiums, which attack them regioselectively to yield, after electrophilic quench, substituted cyclohexadienes.",

author = "Jonathan Clayden and Foricher, \{Yann J Y\} and Lam, \{Ho Kam\}",

year = "2002",

month = aug,

day = "22",

doi = "10.1039/B206479K",

language = "English",

pages = "2138--2139",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "18",

}

TY - JOUR

T1 - Carbolithiation of aromatic rings

T2 - Cyclohexadienes from N-aroyl-2,2,6,6-tetramethylpiperidines

AU - Clayden, Jonathan

AU - Foricher, Yann J Y

AU - Lam, Ho Kam

PY - 2002/8/22

Y1 - 2002/8/22

N2 - Benzamides whose nitrogen atom is part of a 2,2,6,6-tetramethylpiperidine ring are dearomatised by alkyllithiums, which attack them regioselectively to yield, after electrophilic quench, substituted cyclohexadienes.

AB - Benzamides whose nitrogen atom is part of a 2,2,6,6-tetramethylpiperidine ring are dearomatised by alkyllithiums, which attack them regioselectively to yield, after electrophilic quench, substituted cyclohexadienes.

UR - https://www.scopus.com/pages/publications/0036399185

U2 - 10.1039/B206479K

DO - 10.1039/B206479K

M3 - Article (Academic Journal)

C2 - 12357813

AN - SCOPUS:0036399185

SN - 1359-7345

SP - 2138

EP - 2139

JO - Chemical Communications

JF - Chemical Communications

IS - 18

ER -

Carbolithiation of aromatic rings: Cyclohexadienes from N-aroyl-2,2,6,6-tetramethylpiperidines

Abstract

Research Groups and Themes

Access to Document

Handle.net

Other files and links

Fingerprint

Cite this