Total Synthesis of Lycoricidine and Narciclasine by Chemical Dearomatization of Bromobenzene. (Q48199388)

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7 April 2020

title

Total Synthesis of Lycoricidine and Narciclasine by Chemical Dearomatization of Bromobenzene (English)

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7 April 2020

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3

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7 April 2020

author name string

Emma H Southgate

series ordinal

1

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7 April 2020

Daniel R Holycross

series ordinal

2

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7 April 2020

language of work or name

English

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publication date

23 October 2017

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Angewandte Chemie International Edition

7 April 2020

published in

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7 April 2020

volume

56

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7 April 2020

issue

47

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7 April 2020

page(s)

15049-15052

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Arenophile-Mediated Dearomative Reduction.

7 April 2020

cites work

1 reference

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TOTAL SYNTHESES OF PANCRATISTATIN. A REVIEW.

29 September 2018

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Stereo- and regioselectivity of the hetero-Diels-Alder reaction of nitroso derivatives with conjugated dienes

29 September 2018

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Dearomative dihydroxylation with arenophiles.

29 September 2018

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Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: The missing link

29 September 2018

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Synthesis of Amaryllidaceae Constituents and Unnatural Derivatives

29 September 2018

1 reference

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Catalytic Enantioselective Nitroso Diels-Alder Reaction.

29 September 2018

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Regio- and stereochemical studies on the nitroso-Diels-Alder reaction with 1,2-disubstituted dienes

29 September 2018

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Dearomatization strategies in the synthesis of complex natural products

29 September 2018

1 reference

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Synthesis of (+)-lycoricidine by the application of oxidative and regioselective ring-opening of aziridines

29 September 2018

1 reference

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Regioselectivity and stereoselectivity of dioxygenase catalysed cis-dihydroxylation of mono- and tri-cyclic azaarene substrates.

29 September 2018

1 reference

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Amaryllidaceae isocarbostyril alkaloids and their derivatives as promising antitumor agents

29 September 2018

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Chemistry, biology, and medicinal potential of narciclasine and its congeners

29 September 2018

1 reference

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Synthesis of some members of the hydroxylated phenanthridone subclass of the Amaryllidaceae alkaloid family

29 September 2018

1 reference

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Total synthesis and biological evaluation of Amaryllidaceae alkaloids: narciclasine, ent-7-deoxypancratistatin, regioisomer of 7-deoxypancratistatin, 10b-epi-deoxypancratistatin, and truncated derivatives

29 September 2018

1 reference

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A short synthesis of (+)-narciclasine via a strategy derived from stereocontrolled epoxide formation and SnCl(4)-catalyzed arene-epoxide coupling

29 September 2018

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Dihydroxylation of Polyenes Using Narasaka's Modification of the Upjohn Procedure

29 September 2018

1 reference

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Transition states and mechanisms of the hetero-Diels-Alder reactions of hyponitrous acid, nitrosoalkanes, nitrosoarenes, and nitrosocarbonyl compounds

29 September 2018

1 reference

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Substrate specificity of naphthalene dioxygenase: effect of specific amino acids at the active site of the enzyme

29 September 2018

1 reference

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Dihydroxylation and dechlorination of chlorinated biphenyls by purified biphenyl 2,3-dioxygenase from Pseudomonas sp. strain LB400

29 September 2018

1 reference

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Direct Hydroxylation and Amination of Arenes via Deprotonative Cupration

29 September 2018

1 reference

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Lycoricidinol and lycoricidine, new plant-growth regulators in the bulbs of Lycoris radiata herb

1 December 2018

1 reference

12 December 2020

Narciclasine: an Antimitotic Substance from Narcissus Bulbs

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12 December 2020

Antineoplastic agents, 105. Zephyranthes grandiflora

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12 December 2020

Chemoenzymatic approaches to lycorine-type Amaryllidaceae alkaloids: total syntheses of ent-lycoricidine, 3-epi-ent-lycoricidine, and 4-deoxy-3-epi-ent-lycoricidine

1 reference

12 December 2020

Amaryllidaceae and Sceletium alkaloids

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12 December 2020

Identifiers

DOI

10.1002/ANIE.201709712

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29024240%20AND%20SRC:MED&resulttype=core&format=json

7 April 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29024240%20AND%20SRC:MED&resulttype=core&format=json

7 April 2020

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