Diastereoselective Synthesis of Cyclopenta (c) furans by a Catalytic Multicomponent Reaction

to related objects

Abstract: A diastereoselective three‐component reaction between alkynyl enones, aldehydes and secondary amines is reported. With the aid of a benign indium catalyst, a range of highly substituted cyclopenta[c]furan derivatives can be obtained in a single‐step procedure. The formation of the stereodefined heterocyclic motifs takes place via in situ generation of enamines followed by two sequential cyclization steps.

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Diastereoselective Synthesis of Cyclopenta (c) furans by a Catalytic Multicomponent Reaction ; volume:128 ; number:39 ; year:2016 ; pages:12042-12045 ; extent:4
Angewandte Chemie ; 128, Heft 39 (2016), 12042-12045 (gesamt 4)

Creator: Pathipati, Stalin R.
van der Werf, Angela
Eriksson, Lars
Selander, Nicklas

DOI: 10.1002/ange.201606108

URN: urn:nbn:de:101:1-2022101008343499422597

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:32 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Pathipati, Stalin R.
van der Werf, Angela
Eriksson, Lars
Selander, Nicklas

Other Objects (12)

Diastereoselective Synthesis of Cyclopenta (c) furans by a Catalytic Multicomponent Reaction

Diastereoselective Synthesis of Cyclopenta (c) furans by a Catalytic Multicomponent Reaction

Diastereoselective Catalytic C-H Amination

Diastereoselective Catalytic C-H Amination

Diastereoselective Synthesis and Catalytic Activity of Two Chiral cis ‐Dioxidomolybdenum (VI) Complexes

Diastereoselective Synthesis and Catalytic Activity of Two Chiral cis ‐Dioxidomolybdenum (VI) Complexes

Diastereoselective Synthesis of Pyridone ribo‐ C ‐Nucleosides via Heck Reaction and Oxidation

Diastereoselective Synthesis of Pyridone ribo‐ C ‐Nucleosides via Heck Reaction and Oxidation

Diastereoselective synthesis of pyridone ribo‐C‐nucleosides via Heck reaction and oxidation

Diastereoselective synthesis of pyridone ribo‐C‐nucleosides via Heck reaction and oxidation

Cobalt-Catalyzed Enantio- and Diastereoselective Hydroacylation Reaction

Cobalt-Catalyzed Enantio- and Diastereoselective Hydroacylation Reaction

Temperature-Controlled Diastereoselective Doebner/Ugi Tandem Reaction

Temperature-Controlled Diastereoselective Doebner/Ugi Tandem Reaction

The First Enantioselective and Diastereoselective Catalytic Nitro-Mannich Reaction: A New Entry to Chiral Vicinal Diamines

The First Enantioselective and Diastereoselective Catalytic Nitro-Mannich Reaction: A New Entry to Chiral Vicinal Diamines

An Unusual Diastereoselective Pictet–Spengler Reaction: Synthesis of Novel Tetrahydro-β-Carboline Glycosides

An Unusual Diastereoselective Pictet–Spengler Reaction: Synthesis of Novel Tetrahydro-β-Carboline Glycosides

Diastereoselective Synthesis of Pyrrolidines and Prolines

Diastereoselective Synthesis of Pyrrolidines and Prolines

Diastereoselective Synthesis of Cyclopentyl-amines from Aminocyclopropanes

Diastereoselective Synthesis of Cyclopentyl-amines from Aminocyclopropanes

Concise Diastereoselective Total Synthesis of (±)-Parvistemonine A

Concise Diastereoselective Total Synthesis of (±)-Parvistemonine A

Diastereoselective Synthesis of Cyclopenta (c) furans by a Catalytic Multicomponent Reaction

Diastereoselective Synthesis of Cyclopenta (c) furans by a Catalytic Multicomponent Reaction

Diastereoselective Catalytic C-H Amination

Diastereoselective Catalytic C-H Amination

Diastereoselective Synthesis and Catalytic Activity of Two Chiral cis ‐Dioxidomolybdenum (VI) Complexes

Diastereoselective Synthesis and Catalytic Activity of Two Chiral cis ‐Dioxidomolybdenum (VI) Complexes

Diastereoselective Synthesis of Pyridone ribo‐ C ‐Nucleosides via Heck Reaction and Oxidation

Diastereoselective Synthesis of Pyridone ribo‐ C ‐Nucleosides via Heck Reaction and Oxidation

Diastereoselective synthesis of pyridone ribo‐C‐nucleosides via Heck reaction and oxidation

Diastereoselective synthesis of pyridone ribo‐C‐nucleosides via Heck reaction and oxidation

Cobalt-Catalyzed Enantio- and Diastereoselective Hydroacylation Reaction

Cobalt-Catalyzed Enantio- and Diastereoselective Hydroacylation Reaction

Temperature-Controlled Diastereoselective Doebner/Ugi Tandem Reaction

Temperature-Controlled Diastereoselective Doebner/Ugi Tandem Reaction

The First Enantioselective and Diastereoselective Catalytic Nitro-Mannich Reaction: A New Entry to Chiral Vicinal Diamines

The First Enantioselective and Diastereoselective Catalytic Nitro-Mannich Reaction: A New Entry to Chiral Vicinal Diamines

An Unusual Diastereoselective Pictet–Spengler Reaction: Synthesis of Novel Tetrahydro-β-Carboline Glycosides

An Unusual Diastereoselective Pictet–Spengler Reaction: Synthesis of Novel Tetrahydro-β-Carboline Glycosides

Diastereoselective Synthesis of Pyrrolidines and Prolines

Diastereoselective Synthesis of Pyrrolidines and Prolines

Diastereoselective Synthesis of Cyclopentyl-amines from Aminocyclopropanes

Diastereoselective Synthesis of Cyclopentyl-amines from Aminocyclopropanes

Concise Diastereoselective Total Synthesis of (±)-Parvistemonine A

Concise Diastereoselective Total Synthesis of (±)-Parvistemonine A

Diastereoselective Synthesis of Cyclopenta (c) furans by a Catalytic Multicomponent Reaction

Diastereoselective Synthesis of Cyclopenta (c) furans by a Catalytic Multicomponent Reaction

Diastereoselective Catalytic C-H Amination

Diastereoselective Catalytic C-H Amination

Diastereoselective Synthesis and Catalytic Activity of Two Chiral cis ‐Dioxidomolybdenum (VI) Complexes

Diastereoselective Synthesis and Catalytic Activity of Two Chiral cis ‐Dioxidomolybdenum (VI) Complexes

Diastereoselective Synthesis of Pyridone ribo‐ C ‐Nucleosides via Heck Reaction and Oxidation

Diastereoselective Synthesis of Pyridone ribo‐ C ‐Nucleosides via Heck Reaction and Oxidation

Diastereoselective synthesis of pyridone ribo‐C‐nucleosides via Heck reaction and oxidation

Diastereoselective synthesis of pyridone ribo‐C‐nucleosides via Heck reaction and oxidation

Cobalt-Catalyzed Enantio- and Diastereoselective Hydroacylation Reaction

Cobalt-Catalyzed Enantio- and Diastereoselective Hydroacylation Reaction

Temperature-Controlled Diastereoselective Doebner/Ugi Tandem Reaction

Temperature-Controlled Diastereoselective Doebner/Ugi Tandem Reaction

The First Enantioselective and Diastereoselective Catalytic Nitro-Mannich Reaction: A New Entry to Chiral Vicinal Diamines

The First Enantioselective and Diastereoselective Catalytic Nitro-Mannich Reaction: A New Entry to Chiral Vicinal Diamines

An Unusual Diastereoselective Pictet–Spengler Reaction: Synthesis of Novel Tetrahydro-β-Carboline Glycosides

An Unusual Diastereoselective Pictet–Spengler Reaction: Synthesis of Novel Tetrahydro-β-Carboline Glycosides

Diastereoselective Synthesis of Pyrrolidines and Prolines

Diastereoselective Synthesis of Pyrrolidines and Prolines

Diastereoselective Synthesis of Cyclopentyl-amines from Aminocyclopropanes

Diastereoselective Synthesis of Cyclopentyl-amines from Aminocyclopropanes

Concise Diastereoselective Total Synthesis of (±)-Parvistemonine A

Concise Diastereoselective Total Synthesis of (±)-Parvistemonine A

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.