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1
A concise formal synthesis of diazonamide A by the stereoselective construction of the C10 quaternary center.
Angew Chem Int Ed Engl. 2010 Mar 22;49(13):2397-400. doi: 10.1002/anie.200906318.
2
Stereoselective synthesis of the diazonamide a macrocyclic core.
J Org Chem. 2015 Mar 20;80(6):3058-66. doi: 10.1021/jo5029419. Epub 2015 Mar 4.
5
Diazonamide support studies: stereoselective formation of the C10 chiral center in both the CDEFG and AEFG fragments.
Org Lett. 2008 Sep 18;10(18):3969-72. doi: 10.1021/ol8014336. Epub 2008 Aug 15.
7
An approach to the bis-oxazole macrocycle of diazonamides.
Org Lett. 2011 Feb 4;13(3):390-3. doi: 10.1021/ol102678j. Epub 2010 Dec 21.
8
The second total synthesis of diazonamide A.
Angew Chem Int Ed Engl. 2003 Apr 17;42(15):1753-8. doi: 10.1002/anie.200351112.
9
A concise and flexible total synthesis of (-)-diazonamide A.
Angew Chem Int Ed Engl. 2003 Oct 20;42(40):4961-6. doi: 10.1002/anie.200352577.
10
Enantiocontrolled synthesis of a tetracyclic aminal corresponding to the core subunit of diazonamide A.
J Org Chem. 2015 Mar 20;80(6):3050-7. doi: 10.1021/jo502939a. Epub 2015 Mar 5.

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One-Pot Synthesis of Hydroxylated Alkaloids from Sugars via a Pictet-Spengler-Type Reaction.
Molecules. 2024 Dec 3;29(23):5709. doi: 10.3390/molecules29235709.
3
Transition Metal Catalysis Controlled by Hydrogen Bonding in the Second Coordination Sphere.
Chem Rev. 2022 Jul 27;122(14):12308-12369. doi: 10.1021/acs.chemrev.1c00862. Epub 2022 May 20.
4
Unconventional Macrocyclizations in Natural Product Synthesis.
ACS Cent Sci. 2020 Nov 25;6(11):1869-1889. doi: 10.1021/acscentsci.0c00599. Epub 2020 Sep 21.
5
A ,'-dioxide/Mg(OTf) complex catalyzed enantioselective α-addition of isocyanides to alkylidene malonates.
Chem Sci. 2016 Jul 1;7(7):4736-4740. doi: 10.1039/c6sc00689b. Epub 2016 Apr 22.
6
Total synthesis of diazonamide A.
Chem Sci. 2011;2011(2):308-311. doi: 10.1039/C0SC00577K. Epub 2010 Dec 24.
7
Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.
Chem Soc Rev. 2012 Aug 7;41(15):5185-238. doi: 10.1039/c2cs35116a. Epub 2012 Jun 28.
8
Alpha-arylation of 3-aryloxindoles.
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本文引用的文献

4
Diazonamide support studies: stereoselective formation of the C10 chiral center in both the CDEFG and AEFG fragments.
Org Lett. 2008 Sep 18;10(18):3969-72. doi: 10.1021/ol8014336. Epub 2008 Aug 15.
5
Orthogonal Pd- and Cu-based catalyst systems for C- and N-arylation of oxindoles.
J Am Chem Soc. 2008 Jul 23;130(29):9613-20. doi: 10.1021/ja803179s. Epub 2008 Jun 28.
6
The synthetic challenge of diazonamide A, a macrocyclic indole bis-oxazole marine natural product.
Nat Prod Rep. 2008 Apr;25(2):227-53. doi: 10.1039/b705663j. Epub 2008 Jan 11.
7
Palladium-catalyzed alpha-arylation of oxindoles.
Org Lett. 2008 Apr 3;10(7):1413-5. doi: 10.1021/ol800141t. Epub 2008 Mar 6.
10
Diazonamide toxins reveal an unexpected function for ornithine delta-amino transferase in mitotic cell division.
Proc Natl Acad Sci U S A. 2007 Feb 13;104(7):2068-73. doi: 10.1073/pnas.0610832104. Epub 2007 Feb 7.

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