<?xml version="1.0" encoding="UTF-8"?>
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<title>Prof. Manas Chakrabarty</title>
<link href="http://192.168.1.40:8080/xmlui/handle/123456789/1105" rel="alternate"/>
<subtitle/>
<id>http://192.168.1.40:8080/xmlui/handle/123456789/1105</id>
<updated>2026-05-31T13:43:50Z</updated>
<dc:date>2026-05-31T13:43:50Z</dc:date>
<entry>
<title>An expedient, regioselective synthesis of 2-alkylamino- and 2-alkylthiothiazolo[5,4-e]indoles</title>
<link href="http://192.168.1.40:8080/xmlui/handle/123456789/2423" rel="alternate"/>
<author>
<name>Chakrabarty, Manas</name>
</author>
<author>
<name>Kundu, Taraknath</name>
</author>
<author>
<name>Arima, S.</name>
</author>
<author>
<name>Harigaya, Y.</name>
</author>
<id>http://192.168.1.40:8080/xmlui/handle/123456789/2423</id>
<updated>2013-04-02T07:27:25Z</updated>
<published>2005-04-18T00:00:00Z</published>
<summary type="text">An expedient, regioselective synthesis of 2-alkylamino- and 2-alkylthiothiazolo[5,4-e]indoles
Chakrabarty, Manas; Kundu, Taraknath; Arima, S.; Harigaya, Y.
1-Benzenesulfonyl-5-aminoindole 5, prepared from 5-nitroindole 3, was condensed with alkyl isothiocyanates and separately with carbon disulfide and alkyl bromides/iodides to furnish efficiently the corresponding N-alkyl-thioureidoindoles 6a-c and the alkyl N'-(indol-5'-yl)dithiocarbamates 9a-e, respectively. Their cyclisation using N-bromosuccinimide (NBS) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), in the cold, followed by indolic N-deprotection, furnished regioselectively the 2-alkylamino- and the 2-alkylthiothiazolo[5,4-e]indoles 8a-c and 11a-e, respectively, in good overall yields.
DOI: 10.1016/j.tetlet.2005.02.125
</summary>
<dc:date>2005-04-18T00:00:00Z</dc:date>
</entry>
<entry>
<title>A new catalytic application of a keggin acid in the synthesis of symmetrical bis(indolyl)alkanes</title>
<link href="http://192.168.1.40:8080/xmlui/handle/123456789/2421" rel="alternate"/>
<author>
<name>Chakrabarty, Manas</name>
</author>
<author>
<name>Mukherji, Ajanta</name>
</author>
<author>
<name>Karmakar, Sulakshana</name>
</author>
<author>
<name>Arima, S.</name>
</author>
<author>
<name>Harigaya, Y.</name>
</author>
<id>http://192.168.1.40:8080/xmlui/handle/123456789/2421</id>
<updated>2018-11-27T11:50:36Z</updated>
<published>2006-02-01T00:00:00Z</published>
<summary type="text">A new catalytic application of a keggin acid in the synthesis of symmetrical bis(indolyl)alkanes
Chakrabarty, Manas; Mukherji, Ajanta; Karmakar, Sulakshana; Arima, S.; Harigaya, Y.
Silicotungstic acid, H4SiW12O40, an important Keggin heteropoly acid, efficiently catalysed the reaction of indoles with aryl aldehydes in ethyl acetate solution at room temperature to furnish symmetrical bis(indolyl)alkanes expeditiously.
DOI: 10.3987/COM-05-10587
</summary>
<dc:date>2006-02-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>A facile clay-mediated synthesis of 3,3-diindolyl-2-indolinones from isatins</title>
<link href="http://192.168.1.40:8080/xmlui/handle/123456789/2419" rel="alternate"/>
<author>
<name>Chakrabarty, Manas</name>
</author>
<author>
<name>Sarkar, Sandipan</name>
</author>
<author>
<name>Harigaya, Y.</name>
</author>
<id>http://192.168.1.40:8080/xmlui/handle/123456789/2419</id>
<updated>2018-11-27T11:50:34Z</updated>
<published>2005-08-01T00:00:00Z</published>
<summary type="text">A facile clay-mediated synthesis of 3,3-diindolyl-2-indolinones from isatins
Chakrabarty, Manas; Sarkar, Sandipan; Harigaya, Y.
Dry reaction of isatins (3a, 3b) with indoles (4a-e) on montmorillonite K10 clay at room temperature furnished within minutes 3,3-bis(3'-indolyl)-2-indolinones (1a-f) in high yields. 5-Nitroisatin (3c) furnished, in addition to the expected indolinone 1h, 3-hydroxy-3-(3'-indolyl)-5-nitro-2-indolinone (6), a likely intermediate to 1h.
</summary>
<dc:date>2005-08-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>A novel, expedient synthesis of thiazolo[4,5-c]- and -[5,4-b]carbazoles</title>
<link href="http://192.168.1.40:8080/xmlui/handle/123456789/2417" rel="alternate"/>
<author>
<name>Chakrabarty, Manas</name>
</author>
<author>
<name>Ghosh, Nandita</name>
</author>
<author>
<name>Harigaya, Y.</name>
</author>
<id>http://192.168.1.40:8080/xmlui/handle/123456789/2417</id>
<updated>2018-11-27T11:54:10Z</updated>
<published>2004-01-01T00:00:00Z</published>
<summary type="text">A novel, expedient synthesis of thiazolo[4,5-c]- and -[5,4-b]carbazoles
Chakrabarty, Manas; Ghosh, Nandita; Harigaya, Y.
A new synthesis of thiazolo[4,5-c]- and -[5,4-b]carbazoles (6a-e, 7a, 8b-e) was accomplished from 3-aminocarbazoles (3a-e) by separate condensations with methyl and phenyl isothiocyanates, followed by oxidative cyclization of the resulting thioureidocarbazoles (4a-e, 5a).
</summary>
<dc:date>2004-01-01T00:00:00Z</dc:date>
</entry>
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