Chemoselective method for the synthesis of 4-allyl-4-hydroxycyclohexa-2,5-dienone derivatives from 1,4-quinones by an indium-mediated allylation protocol

Dipanjan Pan; Sajal K. Mal; Gandhi K. Kar; Jayanta K. Ray

doi:10.1016/S0040-4020(02)00133-3

Chemoselective method for the synthesis of 4-allyl-4-hydroxycyclohexa-2,5-dienone derivatives from 1,4-quinones by an indium-mediated allylation protocol

Dipanjan Pan
, Sajal K. Mal
, Gandhi K. Kar
, Jayanta K. Ray

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

15 Scopus citations

Abstract

Allyl indium halide on reaction with 1,4-quinones produced 4-allyl-4-hydroxycyclohexa-2,5-dienone derivatives. Unsymmetrical quinones show high chemoselectivity in addition of allyl indium halide reagent to the carbonyl group.

Original language	English (US)
Pages (from-to)	2847-2852
Number of pages	6
Journal	Tetrahedron
Volume	58
Issue number	14
DOIs	https://doi.org/10.1016/S0040-4020(02)00133-3
State	Published - Apr 1 2002

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4020(02)00133-3

Cite this

@article{619ef3c6b35e40968c61b15628d8d916,

title = "Chemoselective method for the synthesis of 4-allyl-4-hydroxycyclohexa-2,5-dienone derivatives from 1,4-quinones by an indium-mediated allylation protocol",

abstract = "Allyl indium halide on reaction with 1,4-quinones produced 4-allyl-4-hydroxycyclohexa-2,5-dienone derivatives. Unsymmetrical quinones show high chemoselectivity in addition of allyl indium halide reagent to the carbonyl group.",

author = "Dipanjan Pan and Mal, \{Sajal K.\} and Kar, \{Gandhi K.\} and Ray, \{Jayanta K.\}",

note = "Funding Information: Financial support from CSIR and DST, New Delhi is gratefully acknowledged.",

year = "2002",

month = apr,

day = "1",

doi = "10.1016/S0040-4020(02)00133-3",

language = "English (US)",

volume = "58",

pages = "2847--2852",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier Ltd",

number = "14",

}

TY - JOUR

T1 - Chemoselective method for the synthesis of 4-allyl-4-hydroxycyclohexa-2,5-dienone derivatives from 1,4-quinones by an indium-mediated allylation protocol

AU - Pan, Dipanjan

AU - Mal, Sajal K.

AU - Kar, Gandhi K.

AU - Ray, Jayanta K.

N1 - Funding Information: Financial support from CSIR and DST, New Delhi is gratefully acknowledged.

PY - 2002/4/1

Y1 - 2002/4/1

N2 - Allyl indium halide on reaction with 1,4-quinones produced 4-allyl-4-hydroxycyclohexa-2,5-dienone derivatives. Unsymmetrical quinones show high chemoselectivity in addition of allyl indium halide reagent to the carbonyl group.

AB - Allyl indium halide on reaction with 1,4-quinones produced 4-allyl-4-hydroxycyclohexa-2,5-dienone derivatives. Unsymmetrical quinones show high chemoselectivity in addition of allyl indium halide reagent to the carbonyl group.

UR - https://www.scopus.com/pages/publications/0036532305

UR - https://www.scopus.com/pages/publications/0036532305#tab=citedBy

U2 - 10.1016/S0040-4020(02)00133-3

DO - 10.1016/S0040-4020(02)00133-3

M3 - Article

AN - SCOPUS:0036532305

SN - 0040-4020

VL - 58

SP - 2847

EP - 2852

JO - Tetrahedron

JF - Tetrahedron

IS - 14

ER -

Chemoselective method for the synthesis of 4-allyl-4-hydroxycyclohexa-2,5-dienone derivatives from 1,4-quinones by an indium-mediated allylation protocol

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this