2016
DOI: 10.1002/anie.201609686
|View full text |Cite
|
Sign up to set email alerts
|

Arenophile‐Mediated Dearomative Reduction

Abstract: A dearomative reduction of simple arenes has been developed which employs a visible-light-mediated cycloaddition of arenes with an N-N-arenophile and in situ diimide reduction. Subsequent cycloreversion or fragmentation of the arenophile moiety affords 1,3-cyclohexadienes or 1,4-diaminocyclohex-2-enes, compounds that are not synthetically accessible using existing dearomatization reactions. Importantly, this strategy also provides numerous opportunities for further derivatization as well as site-selective func… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
30
0
5

Year Published

2017
2017
2021
2021

Publication Types

Select...
7
1

Relationship

3
5

Authors

Journals

citations
Cited by 62 publications
(35 citation statements)
references
References 58 publications
(40 reference statements)
0
30
0
5
Order By: Relevance
“…[7] Specifically, the chemical dihydroxylation of bromobenzene ( 5 ) delivers bromo-3,4-dihydrodiol ( 6 ), a constitutional isomer that is well-suited for the synthesis of lycoricidine ( 1 ) and narciclasine ( 2 ) as the vinyl bromide in 6 is properly situated for appending on the aryl portion of these molecules. Therefore, we envisioned that these natural products could be traced back to bromobenzene ( 5 ) and aryl boronic acid 8 through a Suzuki coupling and two olefin transformations to install the required cis -1,2-diol and 1,4- syn -aminodiol, as shown retrosynthetically in Scheme 2b.…”
mentioning
confidence: 99%
“…[7] Specifically, the chemical dihydroxylation of bromobenzene ( 5 ) delivers bromo-3,4-dihydrodiol ( 6 ), a constitutional isomer that is well-suited for the synthesis of lycoricidine ( 1 ) and narciclasine ( 2 ) as the vinyl bromide in 6 is properly situated for appending on the aryl portion of these molecules. Therefore, we envisioned that these natural products could be traced back to bromobenzene ( 5 ) and aryl boronic acid 8 through a Suzuki coupling and two olefin transformations to install the required cis -1,2-diol and 1,4- syn -aminodiol, as shown retrosynthetically in Scheme 2b.…”
mentioning
confidence: 99%
“…[60] Natürlich hängt die Toleranz gegenüber funktionellen Gruppen von ihren chemischen Eigenschaften ab.V iele Funktionen wie Carbonsäuren/Ester,A mine, [61] Amide und Alkohole/Ether werden häufig toleriert (Abbildung 15). Solche funktionellen Gruppen steigern den Wert der Produkte,d as ie die physikalischen Eigenschaften verändern oder als Ausgangspunkt fürdie Derivatisierung der gesättigten Motive in komplexere Strukturen dienen.…”
Section: Chemoselektive Hydrierung Von Arenen Mit Direkt Angebundenenunclassified
“…So ist generell die Funktionalisierung von Arenen einfacher als die Funktionalisierung der gesättigten Produkte. [60] Natürlich hängt die Toleranz gegenüber funktionellen Gruppen von ihren chemischen Eigenschaften ab.V iele Funktionen wie Carbonsäuren/Ester,A mine, [61] Fluorierte (gesättigte) Verbindungen sind von Interesse fürd ie Agrochemie,f ürP harmazeutika und in der Materialwissenschaft. [63] Weiterhin zeigte die OHagan-Gruppe,d ass all-cis-(multi-)fluorierte Cycloalkane (z.…”
Section: Angewandte Chemieunclassified
“…Sarlah's research involves the discovery of new reactivities and guiding principles for organic synthesis and their application towards biologically active natural products and methods development. His group has described a total synthesis of lycoricidine and narciclasine and an arenophile‐mediated dearomative reduction in Communications in Angewandte Chemie .…”
Section: Awarded …mentioning
confidence: 99%