Green-Bond Forming Reactions. Carbon-Carbon and Carbon-Heteroatom / / ed. by Bubun Banerjee, Rakesh Kumar Sharma.
Carbon-carbon and carbon-heteroatom bond-forming reactions are the backbone of synthetic organic chemistry. Scientists are constantly developing and improving these techniques in order to maximize the diversity of synthetically available molecules. These techniques must be developed in a sustainable...
Wedi'i Gadw mewn:
| Superior document: | Title is part of eBook package: De Gruyter DG Plus DeG Package 2022 Part 1 |
|---|---|
| MitwirkendeR: | |
| HerausgeberIn: | |
| Place / Publishing House: | Berlin ;, Boston : : De Gruyter, , [2022] ©2022 |
| Blwyddyn Gyhoeddi: | 2022 |
| Iaith: | English |
| Cyfres: | Green-Bond Forming Reactions ;
Volume 1 |
| Mynediad Ar-lein: | |
| Disgrifiad Corfforoll: | 1 online resource (XVI, 382 p.) |
| Tagiau: |
Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
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| id |
9783110759549 |
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(DE-B1597)589863 (OCoLC)1343104325 |
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marc |
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Green-Bond Forming Reactions. Carbon-Carbon and Carbon-Heteroatom / ed. by Bubun Banerjee, Rakesh Kumar Sharma. Berlin ; Boston : De Gruyter, [2022] ©2022 1 online resource (XVI, 382 p.) text txt rdacontent computer c rdamedia online resource cr rdacarrier text file PDF rda Green-Bond Forming Reactions ; Volume 1 Frontmatter -- Preface -- Contents -- List of contributing authors -- 1 Recent developments in C–C bond formation catalyzed by solid supported palladium: a greener perspective -- 2 Visible-light-mediated metal-free C–Si bond formation reactions -- 3 Synthesis of antiviral drugs by using carbon–carbon and carbon–heteroatom bond formation under greener conditions -- 4 Green synthesis of triazolo-nucleoside conjugates via azide–alkyne C–N bond formation -- 5 An overview of quinoxaline synthesis by green methods: recent reports -- 6 Green protocols for Tsuji–Trost allylation: an overview -- 7 Recyclable magnetically retrievable nanocatalysts for C–heteroatom bond formation reactions -- 8 Carbocatalysis: a metal free green avenue towards carbon–carbon/heteroatom bond construction -- 9 Use of heterogeneous catalysis in sustainable biofuel production -- 10 Catalytic applications of graphene oxide towards the synthesis of bioactive scaffolds through the formation of carbon– carbon and carbon–heteroatom bonds -- 11 Dicarbonyl compounds in the synthesis of heterocycles under green conditions -- 12 Polyanilinemediated heterogeneous catalysis in the preparation of heterocyclic derivatives through carbon–heteroatom bond formations -- Index restricted access http://purl.org/coar/access_right/c_16ec online access with authorization star Carbon-carbon and carbon-heteroatom bond-forming reactions are the backbone of synthetic organic chemistry. Scientists are constantly developing and improving these techniques in order to maximize the diversity of synthetically available molecules. These techniques must be developed in a sustainable manner in order to limit their environmental impact. This book highlights green carbon-carbon and carbon-heteroatom bond forming reactions. Issued also in print. Mode of access: Internet via World Wide Web. In English. Description based on online resource; title from PDF title page (publisher's Web site, viewed 02. Mai 2023) Grüne Chemie. Katalyse. Nachhaltigkeit. Organische Chemie. SCIENCE / Chemistry / General. bisacsh Bioactive Heterocycles. Bond Formation. C-heteroatom Bonds. Green Chemistry. Green Synthesis. Organic Chemistry. Sustainable Developments, Carbon-Carbon Bonds. Sustainable Synthesis. Allaka, Tejeswara Rao, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Banerjee, Bubun, editor. edt http://id.loc.gov/vocabulary/relators/edt Basak, Puja, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Basu, Basudeb, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Bhattacharya, Suchandra, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Dandia, Anshu, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Dapper, Luiz H., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Dixit, Ranjana, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Durga Nageswar, Yadavalli Venkata, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Dutta, Sriparna, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Ghosh, Pranab, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Ghosh, Sumit, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Hajra, Alakananda, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Hartwig, Daniela, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Hassan, Amal I., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Jonnalagadda, Sreekanth Babu, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb João Lenardão, Eder, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Katari, Naresh Kumar, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Katla, Ramesh, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Kumar Sharma, Rakesh, editor. edt http://id.loc.gov/vocabulary/relators/edt Kumar, Krishan, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Kumar, Manish, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Kumar, Prashant, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Kumar, Rajesh, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Kumar, Sandeep, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Maity, Jyotirmoy, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Mathur, Divya, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Mukhopadhyay, Chhanda, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Nascimento, José E. R., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Parewa, Vijay, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Parihar, Sonam, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Prasad, Ashok K., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Rana, Neha, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Rao Vaidya, Jayathirtha, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Saha, Debasree, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Saini, Surendra, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Saleh, Hosam M., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Sharma, Rakesh Kumar, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Singha, Rabindranath, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Soares, Liane K., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Verma, Abhishek, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Yadav, Sneha, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Title is part of eBook package: De Gruyter DG Plus DeG Package 2022 Part 1 9783110766820 Title is part of eBook package: De Gruyter EBOOK PACKAGE COMPLETE 2022 English 9783110993899 Title is part of eBook package: De Gruyter EBOOK PACKAGE COMPLETE 2022 9783110994810 ZDB-23-DGG Title is part of eBook package: De Gruyter EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2022 English 9783110993448 Title is part of eBook package: De Gruyter EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2022 9783110993219 ZDB-23-DPC EPUB 9783110759594 print 9783110759495 https://doi.org/10.1515/9783110759549 https://www.degruyter.com/isbn/9783110759549 Cover https://www.degruyter.com/document/cover/isbn/9783110759549/original |
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Allaka, Tejeswara Rao, |
| title |
Green-Bond Forming Reactions. Carbon-Carbon and Carbon-Heteroatom / |
| spellingShingle |
Green-Bond Forming Reactions. Carbon-Carbon and Carbon-Heteroatom / Green-Bond Forming Reactions ; Frontmatter -- Preface -- Contents -- List of contributing authors -- 1 Recent developments in C–C bond formation catalyzed by solid supported palladium: a greener perspective -- 2 Visible-light-mediated metal-free C–Si bond formation reactions -- 3 Synthesis of antiviral drugs by using carbon–carbon and carbon–heteroatom bond formation under greener conditions -- 4 Green synthesis of triazolo-nucleoside conjugates via azide–alkyne C–N bond formation -- 5 An overview of quinoxaline synthesis by green methods: recent reports -- 6 Green protocols for Tsuji–Trost allylation: an overview -- 7 Recyclable magnetically retrievable nanocatalysts for C–heteroatom bond formation reactions -- 8 Carbocatalysis: a metal free green avenue towards carbon–carbon/heteroatom bond construction -- 9 Use of heterogeneous catalysis in sustainable biofuel production -- 10 Catalytic applications of graphene oxide towards the synthesis of bioactive scaffolds through the formation of carbon– carbon and carbon–heteroatom bonds -- 11 Dicarbonyl compounds in the synthesis of heterocycles under green conditions -- 12 Polyanilinemediated heterogeneous catalysis in the preparation of heterocyclic derivatives through carbon–heteroatom bond formations -- Index |
| title_full |
Green-Bond Forming Reactions. Carbon-Carbon and Carbon-Heteroatom / ed. by Bubun Banerjee, Rakesh Kumar Sharma. |
| title_fullStr |
Green-Bond Forming Reactions. Carbon-Carbon and Carbon-Heteroatom / ed. by Bubun Banerjee, Rakesh Kumar Sharma. |
| title_full_unstemmed |
Green-Bond Forming Reactions. Carbon-Carbon and Carbon-Heteroatom / ed. by Bubun Banerjee, Rakesh Kumar Sharma. |
| title_auth |
Green-Bond Forming Reactions. Carbon-Carbon and Carbon-Heteroatom / |
| title_alt |
Frontmatter -- Preface -- Contents -- List of contributing authors -- 1 Recent developments in C–C bond formation catalyzed by solid supported palladium: a greener perspective -- 2 Visible-light-mediated metal-free C–Si bond formation reactions -- 3 Synthesis of antiviral drugs by using carbon–carbon and carbon–heteroatom bond formation under greener conditions -- 4 Green synthesis of triazolo-nucleoside conjugates via azide–alkyne C–N bond formation -- 5 An overview of quinoxaline synthesis by green methods: recent reports -- 6 Green protocols for Tsuji–Trost allylation: an overview -- 7 Recyclable magnetically retrievable nanocatalysts for C–heteroatom bond formation reactions -- 8 Carbocatalysis: a metal free green avenue towards carbon–carbon/heteroatom bond construction -- 9 Use of heterogeneous catalysis in sustainable biofuel production -- 10 Catalytic applications of graphene oxide towards the synthesis of bioactive scaffolds through the formation of carbon– carbon and carbon–heteroatom bonds -- 11 Dicarbonyl compounds in the synthesis of heterocycles under green conditions -- 12 Polyanilinemediated heterogeneous catalysis in the preparation of heterocyclic derivatives through carbon–heteroatom bond formations -- Index |
| title_new |
Green-Bond Forming Reactions. Carbon-Carbon and Carbon-Heteroatom / |
| title_sort |
green-bond forming reactions. carbon-carbon and carbon-heteroatom / |
| series |
Green-Bond Forming Reactions ; |
| series2 |
Green-Bond Forming Reactions ; |
| publisher |
De Gruyter, |
| publishDate |
2022 |
| physical |
1 online resource (XVI, 382 p.) Issued also in print. |
| contents |
Frontmatter -- Preface -- Contents -- List of contributing authors -- 1 Recent developments in C–C bond formation catalyzed by solid supported palladium: a greener perspective -- 2 Visible-light-mediated metal-free C–Si bond formation reactions -- 3 Synthesis of antiviral drugs by using carbon–carbon and carbon–heteroatom bond formation under greener conditions -- 4 Green synthesis of triazolo-nucleoside conjugates via azide–alkyne C–N bond formation -- 5 An overview of quinoxaline synthesis by green methods: recent reports -- 6 Green protocols for Tsuji–Trost allylation: an overview -- 7 Recyclable magnetically retrievable nanocatalysts for C–heteroatom bond formation reactions -- 8 Carbocatalysis: a metal free green avenue towards carbon–carbon/heteroatom bond construction -- 9 Use of heterogeneous catalysis in sustainable biofuel production -- 10 Catalytic applications of graphene oxide towards the synthesis of bioactive scaffolds through the formation of carbon– carbon and carbon–heteroatom bonds -- 11 Dicarbonyl compounds in the synthesis of heterocycles under green conditions -- 12 Polyanilinemediated heterogeneous catalysis in the preparation of heterocyclic derivatives through carbon–heteroatom bond formations -- Index |
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Not Illustrated |
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500 - Science |
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540 - Chemistry |
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540 - Chemistry & allied sciences |
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540 |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>09294nam a22013815i 4500</leader><controlfield tag="001">9783110759549</controlfield><controlfield tag="003">DE-B1597</controlfield><controlfield tag="005">20230502090707.0</controlfield><controlfield tag="006">m|||||o||d||||||||</controlfield><controlfield tag="007">cr || ||||||||</controlfield><controlfield tag="008">230502t20222022gw fo d z eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9783110759549</subfield></datafield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1515/9783110759549</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-B1597)589863</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)1343104325</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-B1597</subfield><subfield code="b">eng</subfield><subfield code="c">DE-B1597</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="044" ind1=" " ind2=" "><subfield code="a">gw</subfield><subfield code="c">DE</subfield></datafield><datafield tag="072" ind1=" " ind2="7"><subfield code="a">SCI013000</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">DE-101</subfield></datafield><datafield tag="245" ind1="0" ind2="0"><subfield code="a">Green-Bond Forming Reactions. Carbon-Carbon and Carbon-Heteroatom /</subfield><subfield code="c">ed. by Bubun Banerjee, Rakesh Kumar Sharma.</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Berlin ;</subfield><subfield code="a">Boston : </subfield><subfield code="b">De Gruyter, </subfield><subfield code="c">[2022]</subfield></datafield><datafield tag="264" ind1=" " ind2="4"><subfield code="c">©2022</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 online resource (XVI, 382 p.)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="347" ind1=" " ind2=" "><subfield code="a">text file</subfield><subfield code="b">PDF</subfield><subfield code="2">rda</subfield></datafield><datafield tag="490" ind1="0" ind2=" "><subfield code="a">Green-Bond Forming Reactions ;</subfield><subfield code="v">Volume 1</subfield></datafield><datafield tag="505" ind1="0" ind2="0"><subfield code="t">Frontmatter -- </subfield><subfield code="t">Preface -- </subfield><subfield code="t">Contents -- </subfield><subfield code="t">List of contributing authors -- </subfield><subfield code="t">1 Recent developments in C–C bond formation catalyzed by solid supported palladium: a greener perspective -- </subfield><subfield code="t">2 Visible-light-mediated metal-free C–Si bond formation reactions -- </subfield><subfield code="t">3 Synthesis of antiviral drugs by using carbon–carbon and carbon–heteroatom bond formation under greener conditions -- </subfield><subfield code="t">4 Green synthesis of triazolo-nucleoside conjugates via azide–alkyne C–N bond formation -- </subfield><subfield code="t">5 An overview of quinoxaline synthesis by green methods: recent reports -- </subfield><subfield code="t">6 Green protocols for Tsuji–Trost allylation: an overview -- </subfield><subfield code="t">7 Recyclable magnetically retrievable nanocatalysts for C–heteroatom bond formation reactions -- </subfield><subfield code="t">8 Carbocatalysis: a metal free green avenue towards carbon–carbon/heteroatom bond construction -- </subfield><subfield code="t">9 Use of heterogeneous catalysis in sustainable biofuel production -- </subfield><subfield code="t">10 Catalytic applications of graphene oxide towards the synthesis of bioactive scaffolds through the formation of carbon– carbon and carbon–heteroatom bonds -- </subfield><subfield code="t">11 Dicarbonyl compounds in the synthesis of heterocycles under green conditions -- </subfield><subfield code="t">12 Polyanilinemediated heterogeneous catalysis in the preparation of heterocyclic derivatives through carbon–heteroatom bond formations -- </subfield><subfield code="t">Index</subfield></datafield><datafield tag="506" ind1="0" ind2=" "><subfield code="a">restricted access</subfield><subfield code="u">http://purl.org/coar/access_right/c_16ec</subfield><subfield code="f">online access with authorization</subfield><subfield code="2">star</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Carbon-carbon and carbon-heteroatom bond-forming reactions are the backbone of synthetic organic chemistry. Scientists are constantly developing and improving these techniques in order to maximize the diversity of synthetically available molecules. These techniques must be developed in a sustainable manner in order to limit their environmental impact. This book highlights green carbon-carbon and carbon-heteroatom bond forming reactions.</subfield></datafield><datafield tag="530" ind1=" " ind2=" "><subfield code="a">Issued also in print.</subfield></datafield><datafield tag="538" ind1=" " ind2=" "><subfield code="a">Mode of access: Internet via World Wide Web.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">In English.</subfield></datafield><datafield tag="588" ind1="0" ind2=" "><subfield code="a">Description based on online resource; title from PDF title page (publisher's Web site, viewed 02. Mai 2023)</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Grüne Chemie.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Katalyse.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Nachhaltigkeit.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Organische Chemie.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SCIENCE / Chemistry / General.</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Bioactive Heterocycles.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Bond Formation.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">C-heteroatom Bonds.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Green Chemistry.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Green Synthesis.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Organic Chemistry.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Sustainable Developments, Carbon-Carbon Bonds.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Sustainable Synthesis.</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Allaka, Tejeswara Rao, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Banerjee, Bubun, </subfield><subfield code="e">editor.</subfield><subfield code="4">edt</subfield><subfield code="4">http://id.loc.gov/vocabulary/relators/edt</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Basak, Puja, </subfield><subfield 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