1984
DOI: 10.1021/ja00330a061
|View full text |Cite
|
Sign up to set email alerts
|

The reaction of alkynes with (ethoxyalkylidene)tetracarbonyliron(0) complexes

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
10
0

Year Published

1991
1991
2009
2009

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 39 publications
(10 citation statements)
references
References 0 publications
0
10
0
Order By: Relevance
“…Thus, (alkoxycarbene)iron complexes are known to form fourcomponent pyrones [9] by treatment with alkynes while the analogous reaction with (aminocarbene)iron complexes produces three-component amino-furans [10]. Regarding group 6 FCCs, the Dö tz benzannulation is a [3 + 2 + 1] cyclization between an alkenyl or aryl carbene and an alkyne to form an aromatic ring where three carbon atoms of the carbene ligand, the two acetylenic carbons and a carbonyl ligand are joined together.…”
Section: Reactions Initiated By Alkyne Insertionmentioning
confidence: 99%
“…Thus, (alkoxycarbene)iron complexes are known to form fourcomponent pyrones [9] by treatment with alkynes while the analogous reaction with (aminocarbene)iron complexes produces three-component amino-furans [10]. Regarding group 6 FCCs, the Dö tz benzannulation is a [3 + 2 + 1] cyclization between an alkenyl or aryl carbene and an alkyne to form an aromatic ring where three carbon atoms of the carbene ligand, the two acetylenic carbons and a carbonyl ligand are joined together.…”
Section: Reactions Initiated By Alkyne Insertionmentioning
confidence: 99%
“…The overall yields of the complexed pyrones (11,14,15) were poor, typically 0-10%, with substantial amounts of starting materials recovered. To our surprise, varying amounts of the hydrodebrominated products (7,12,15) were formed in all the reactions. There are a number of reports on the reduction of Csp 3 -X bonds by Fe 2 (CO) 9 .…”
mentioning
confidence: 88%
“…Iron-alkylidene complexes 2 react with symmetrical and unsymmetrical alkynes, for which the latter is highly regioselective, to afford derivatives of 1. 7 h 3 -Acryloyl-iron complexes 3 8 are known to react with SFO 2 (OMe), 9 which in the presence of CO, form the complexed pyrone. Thermal rearrangements via a (h 3 -vinylcarbene)iron complex and a 1,4-oxygen shift, however complicates this method.…”
mentioning
confidence: 99%
“…The credit for the development and application of organoiron complexes in organic and organometallic chemistry can be ascribed to brilliant contributions by Fischer [ 32 , 33 ], Pettit [ 34 ], Müller [ 35 ], Alper [ 10 ], King [ 36 ], Rosenblum [ 37 40 ], Brunner [ 41 ], Birch [ 14 ], Collman [ 42 ], Gompper [ 43 ], Sarel [ 44 ], Noyori [ 45 , 46 ], Pearson [ 20 , 21 ], Casey [ 47 ], Hegedus [ 13 ], Wojcicki [ 48 ], Reger [ 49 ], Helquist [ 50 ], Gladysz [ 51 ], Kerber [ 52 ], Wulff [ 53 ], Ojima [ 54 ], Negishi [ 55 ], Backvall [ 56 ], Herndon [ 57 ], von Gustorf [ 58 ], Grée [ 30 ], Seyferth [ 59 ], Davies [ 60 – 63 ], Liebeskind [ 64 ], Semmelhack [ 65 ], Brookhart [ 66 ], and others [ 31 , 67 73 ]. Credit is also due Fischer [ 24 ], Dötz [ 74 ], Jaouen [ 18 ], Semmelhack [ 19 ], Wulff [ 53 , 75 ] Hegedus [ 76 ], Yamashita [ 77 ], and others [ 77a , 77b ] for their st...…”
Section: Scope Of the Reviewmentioning
confidence: 99%