Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q45714595)
Watch
English
A practical route to enantiopure, highly functionalized seven-membered carbocycles and tetrahydrofurans: concise synthesis of (+)-nemorensic Acid.
scientific article published in February 2002
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
title
A practical route to enantiopure, highly functionalized seven-membered carbocycles and tetrahydrofurans: concise synthesis of (+)-nemorensic Acid
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author
Fernando López
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
José L Mascareñas
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author name string
Luis Castedo
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
language of work or name
English
0 references
publication date
1 February 2002
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
published in
Chemistry—A European Journal
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
volume
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
page(s)
884-899
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
cites work
The atom economy--a search for synthetic efficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Atom Economy—A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Exploration of fundamental and synthetic aspects of the intramolecular 4 + 3 cycloaddition reaction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
The first intermolecular transition metal-catalyzed [5+2] cycloadditions with simple, unactivated, vinylcyclopropanes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Chiral allyl cations are captured by furan with 100% stereoselectivity: synthesis of enantiopure 2-alkoxy-8-oxabicyclo
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Reversal of stereoselectivity in [5 + 2] pyrone--alkene cycloadditons using a sulfoxide-to-sulfoximine switch. Enantiodivergent synthesis of 8-oxabicyclo[3.2.1]octane systems.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
An enantioselective synthesis and biobehavioral evaluation of 7-fluoro-3-(p-fluorophenyl)-2-propyltropanes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Allylic 1,3-strain as a controlling factor in stereoselective transformations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Highly enantioselective hetero-Diels-Alder reactions catalyzed by a C(2)-symmetric bis(sulfoximine) copper(II) complex.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Conformations of Chiral α,β-Unsaturated Sulfoxides and Their Complexes with Lewis Acids. An ab Initio Study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Chemists clean up synthesis with one-pot reactions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Stereocontrolled Routes to Bridged Ethers by Tandem Cyclizations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Transition Metal Catalyzed [5 + 2] Cycloadditions of Vinylcyclopropanes and Alkynes: A Homolog of the Diels-Alder Reaction for the Synthesis of Seven-Membered Rings
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Straightforward Construction of Fused 6,7,5-Tricarbocyclic Systems by Tandem [5 + 2]/[4 + 2] Cycloadditions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Unmasking the 6,7,5-tricarbocyclic frame of
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Aggregated intermediates in the aldol reaction sequence. Crystal structure of the open dimer of LiTMP.cntdot.TMEDA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Chiral Allyl Cations in Cycloadditions to Furan: Synthesis of 2-(1'-Phenylethoxy)-8-oxabicyclo[3.2.1]oct-6-en-3-one in High Enantiomeric Purity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
High regio-, chemo-, and stereoselectivity via low-temperature 4 + 3 cycloadditions. Convergent synthesis of multifunctionalized vinylmetals (M = Si, Sn) and S-vinyl benzenecarbothioates
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Diastereocontrol of [4 + 3] Cyclic Oxyallyl Cycloadditions by Alkoxy Substituents
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Sulfinyl-directed diastereoselective
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Toward an understanding of the mechanisms of the intramolecular
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Enantiospecific Synthesis of (+)-Nemorensic Acid, a Necic Acid Component of the Macropyrrolizidine Alkaloid, Nemorensine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1521-3765%2820020215%298%3A4%3C884%3A%3AAID-CHEM884%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Identifiers
DOI
10.1002/1521-3765(20020215)8:4<884::AID-CHEM884>3.0.CO;2-Q
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
PubMed publication ID
11857703
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11857703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11857703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit