相似文献
1
Uniting anion relay chemistry with Pd-mediated cross coupling: design, synthesis and evaluation of bifunctional aryl and vinyl silane linchpins.
Org Lett. 2010 Feb 5;12(3):588-91. doi: 10.1021/ol902784q.
2
Type II Anion Relay Chemistry: Conformational Constraints To Achieve Effective [1,5]-Vinyl Brook Rearrangements.
J Am Chem Soc. 2017 Jun 28;139(25):8710-8717. doi: 10.1021/jacs.7b04149. Epub 2017 Jun 14.
3
Long-range anion relay chemistry (LR-ARC): a validated ARC tactic.
Org Lett. 2012 Dec 21;14(24):6314-7. doi: 10.1021/ol303080h. Epub 2012 Dec 6.
4
Benzyl and phenylthiomethyl silanes: a new class of bifunctional linchpins for type II anion relay chemistry (ARC).
Org Lett. 2010 Mar 19;12(6):1260-3. doi: 10.1021/ol100130x.
5
[1,5]-Anion relay/[2,3]-Wittig rearrangement of 3,3-bis(silyl) allyl enol ethers: synthesis of useful vinyl bis(silane) species.
Org Lett. 2012 Feb 17;14(4):1094-7. doi: 10.1021/ol300004b. Epub 2012 Jan 25.
6
Vicinal functionalization of propiolate esters via catalytic carbocupration: stereoselective formation of substituted vinyl silanes.
Org Lett. 2010 Jun 18;12(12):2750-3. doi: 10.1021/ol100854j.
7
Radical-mediated silyl- and germyldesulfonylation of vinyl and (alpha-fluoro)vinyl sulfones: application of tris(trimethylsilyl)silanes and tris(trimethylsilyl)germanes in Pd-catalyzed couplings.
Org Lett. 2004 Jun 10;6(12):2047-9. doi: 10.1021/ol049312n.
8
Bissilyl enal: a useful linchpin for synthesis of functionalized vinylsilane species by anion relay chemistry.
Org Lett. 2012 Jan 6;14(1):158-61. doi: 10.1021/ol202942a. Epub 2011 Nov 30.
9
Stereoselective Synthesis of - and -Tetrasubstituted Vinyl Silanes Using a Silyl-Heck Strategy and Hiyama Conditions for Their Cross-Coupling.
J Am Chem Soc. 2020 Jul 15;142(28):12051-12055. doi: 10.1021/jacs.0c05382. Epub 2020 Jun 30.
10
Ir(I)/HCl catalyzed head-to-tail homocoupling reactions of vinylsilanes.
Org Lett. 2012 Mar 16;14(6):1468-71. doi: 10.1021/ol300203w. Epub 2012 Feb 24.
引用本文的文献
1
Pd-catalyzed sp-sp cross-coupling of benzyl bromides using lithium acetylides.
Chem Commun (Camb). 2021 Jul 29;57(61):7529-7532. doi: 10.1039/d1cc02762j.
2
Evolution of Anion Relay Chemistry: Construction of Architecturally Complex Natural Products.
Acc Chem Res. 2020 Apr 21;53(4):988-1000. doi: 10.1021/acs.accounts.0c00076. Epub 2020 Apr 9.
3
Engaging Aldehydes in CuH-Catalyzed Reductive Coupling Reactions: Stereoselective Allylation with Unactivated 1,3-Diene Pronucleophiles.
Angew Chem Int Ed Engl. 2019 Nov 18;58(47):17074-17080. doi: 10.1002/anie.201911008. Epub 2019 Oct 22.
4
Synthetic Access to the Mandelalide Family of Macrolides: Development of an Anion Relay Chemistry Strategy.
J Org Chem. 2018 Apr 20;83(8):4287-4306. doi: 10.1021/acs.joc.8b00268. Epub 2018 Feb 26.
5
Anion Relay Chemistry: Development of an Effective Diastereoselective [3+2] Annulation Tactic Exploiting an Aldol/Brook Rearrangement/Cyclization Cascade.
Angew Chem Int Ed Engl. 2017 Nov 6;56(45):14102-14106. doi: 10.1002/anie.201708017. Epub 2017 Oct 10.
6
Type II Anion Relay Chemistry: Conformational Constraints To Achieve Effective [1,5]-Vinyl Brook Rearrangements.
J Am Chem Soc. 2017 Jun 28;139(25):8710-8717. doi: 10.1021/jacs.7b04149. Epub 2017 Jun 14.
7
Total Synthesis of (-)-Mandelalide A Exploiting Anion Relay Chemistry (ARC): Identification of a Type II ARC/CuCN Cross-Coupling Protocol.
J Am Chem Soc. 2016 Mar 23;138(11):3675-8. doi: 10.1021/jacs.6b01731. Epub 2016 Mar 8.
8
An Effective Bifunctional Aldehyde Linchpin for Type II Anion Relay Chemistry: Development and Application to the Synthesis of a C16-C29 Fragment of Rhizopodin.
Org Lett. 2015 Dec 18;17(24):6242-5. doi: 10.1021/acs.orglett.5b03235. Epub 2015 Dec 7.
9
Total Synthesis of (-)-Secu'amamine A Exploiting Type II Anion Relay Chemistry.
Org Lett. 2015 Sep 4;17(17):4232-5. doi: 10.1021/acs.orglett.5b02018. Epub 2015 Aug 20.
10
Long-range anion relay chemistry (LR-ARC): a validated ARC tactic.
Org Lett. 2012 Dec 21;14(24):6314-7. doi: 10.1021/ol303080h. Epub 2012 Dec 6.
本文引用的文献
1
Evolution of multi-component anion relay chemistry (ARC): construction of architecturally complex natural and unnatural products.
Chem Commun (Camb). 2008 Dec 7(45):5883-95. doi: 10.1039/b810394a. Epub 2008 Sep 30.
2
Ortho-TMS benzaldehyde: an effective linchpin for type II anion relay chemistry (ARC).
Angew Chem Int Ed Engl. 2008;47(37):7082-6. doi: 10.1002/anie.200802301.
3
Evolution of dithiane-based strategies for the construction of architecturally complex natural products.
Acc Chem Res. 2004 Jun;37(6):365-77. doi: 10.1021/ar030245r.
4
Target-oriented and diversity-oriented organic synthesis in drug discovery.
Science. 2000 Mar 17;287(5460):1964-9. doi: 10.1126/science.287.5460.1964.
Zotero 插件