Advances in Cross-Coupling Reactions (Record no. 3007292)

MARC details
000 -LEADER
fixed length control field 04658naaaa2200997uu 4500
001 - CONTROL NUMBER
control field https://directory.doabooks.org/handle/20.500.12854/69364
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220714185006.0
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number books978-3-03943-568-5
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9783039435678
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9783039435685
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.3390/books978-3-03943-568-5
Terms of availability doi
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title English
042 ## - AUTHENTICATION CODE
Authentication code dc
072 #7 - SUBJECT CATEGORY CODE
Subject category code GP
Source bicssc
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Pérez Sestelo, José
Relator code edt
9 (RLIN) 1606914
245 10 - TITLE STATEMENT
Title Advances in Cross-Coupling Reactions
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc Basel, Switzerland
Name of publisher, distributor, etc MDPI - Multidisciplinary Digital Publishing Institute
Date of publication, distribution, etc 2020
300 ## - PHYSICAL DESCRIPTION
Extent 1 electronic resource (234 p.)
506 0# - RESTRICTIONS ON ACCESS NOTE
Terms governing access Open Access
Source of term star
Standardized terminology for access restriction Unrestricted online access
520 ## - SUMMARY, ETC.
Summary, etc In this Special Issue, recent advances in cross-coupling reactions are presented in the form of original research articles, reviews, and short communications. These contributions cover different topics in this area, including novel coupling reactions, reaction conditions, synthetic alternatives, metal ligands, and applications for new pharmaceutical compounds and organic materials. In particular, the reviews deal with methodologies such as the synthesis of diarylketones through palladium catalysis and the most relevant examples of Suzuki-Miyaura and Buchwald-Hartwig coupling reactions in the synthesis of bioactive compounds. The synthetic utility of cross-coupling reactions for the synthesis of medium-size rings and the utility of Stille and Suzuki coupling reactions for the synthesis of new molecular machines based on sterically hindered anthracenyl trypticenyl units are also summarized. The original research articles present the synthesis of 2-alkynylpyrrols by inverse Sonogashira coupling and the synthesis of indoles under oxidative dearomative cross-dehydrogenative conditions. The efficient combination of iridium-catalyzed C-H borylation of aryl halides with the Sonogashira coupling and a sequential iridium-catalyzed borylation of NH-free pyrroles followed by a Suzuki-Miyaura reaction are included. The synthesis of aryl propionic acids, a common structural motif in medicinal chemistry, and the synthesis of new organic dyes are also covered.
540 ## - TERMS GOVERNING USE AND REPRODUCTION NOTE
Terms governing use and reproduction Creative Commons
-- https://creativecommons.org/licenses/by/4.0/
-- cc
-- https://creativecommons.org/licenses/by/4.0/
546 ## - LANGUAGE NOTE
Language note English
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Research & information: general
Source of heading or term bicssc
9 (RLIN) 928234
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Uncontrolled term cross coupling
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Uncontrolled term dearomatization
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Uncontrolled term C-H functionalization
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Uncontrolled term indolin-3-ones
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Uncontrolled term dimerization and trimerization of indoles
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Uncontrolled term C-H borylation
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Uncontrolled term Sonogashira cross-coupling
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Uncontrolled term borylated aryl alkynes
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Uncontrolled term one-pot reaction
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Uncontrolled term restricted rotations
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Uncontrolled term M(CO)3 tripods
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Uncontrolled term V-T NMR
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Uncontrolled term borylation
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Uncontrolled term Suzuki coupling
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Uncontrolled term NH-Free
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Uncontrolled term 5-aryl pyrrole-2-carboxylates
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Uncontrolled term iridium-catalyzed
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Uncontrolled term heteroaryl substituted pyrroles
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Uncontrolled term 2,3'-bipyrrole
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Uncontrolled term electrophilic haloacetylenes
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Uncontrolled term pyrroles
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Uncontrolled term ethynylpyrroles
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Uncontrolled term furans
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Uncontrolled term thiophenes
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Uncontrolled term pyrazoles
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Uncontrolled term Al2O3
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Uncontrolled term transition-metal catalysis
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Uncontrolled term intramolecular cyclization
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Uncontrolled term medium-sized heterocycles
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Uncontrolled term C-H activation
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Uncontrolled term acylation
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Uncontrolled term palladium
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Uncontrolled term indigo dyes
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Uncontrolled term DSSC
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Uncontrolled term synthesis
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Uncontrolled term spectroscopy
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Uncontrolled term Heck reaction
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Uncontrolled term styrene
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Uncontrolled term profene
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Uncontrolled term cross-coupling reactions
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Uncontrolled term C-C bond forming reactions
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Uncontrolled term catalysis in water
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Uncontrolled term C-C cross-coupling
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Uncontrolled term Suzuki-Miyaura reaction
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Uncontrolled term sulfonated salan
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Uncontrolled term n/a
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Sarandeses, Luis A.
Relator code edt
9 (RLIN) 1606915
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pérez Sestelo, José
Relator code oth
9 (RLIN) 1606914
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Sarandeses, Luis A.
Relator code oth
9 (RLIN) 1606915
856 40 - ELECTRONIC LOCATION AND ACCESS
Host name www.oapen.org
Uniform Resource Identifier <a href="https://mdpi.com/books/pdfview/book/3157">https://mdpi.com/books/pdfview/book/3157</a>
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Public note DOAB: download the publication
856 40 - ELECTRONIC LOCATION AND ACCESS
Host name www.oapen.org
Uniform Resource Identifier <a href="https://directory.doabooks.org/handle/20.500.12854/69364">https://directory.doabooks.org/handle/20.500.12854/69364</a>
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Public note DOAB: description of the publication
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