173 related articles for article (PubMed ID: 16351123)
1. Fully stereocontrolled total syntheses of the prostacyclin analogues 16S-iloprost and 16S-3-oxa-iloprost by a common route, using alkenylcopper-azoalkene conjugate addition, asymmetric olefination, and allylic alkylation.
Kramp GJ; Kim M; Gais HJ; Vermeeren C
J Am Chem Soc; 2005 Dec; 127(50):17910-20. PubMed ID: 16351123
[TBL] [Abstract][Full Text] [Related]
2. Development of a common fully stereocontrolled access to the medicinally important and promising prostacyclin analogues iloprost, 3-oxa-iloprost and cicaprost.
Gais HJ; Kramp GJ; Wolters D; Reddy LR
Chemistry; 2006 Jul; 12(21):5610-7. PubMed ID: 16708414
[TBL] [Abstract][Full Text] [Related]
3. Fully stereocontrolled syntheses of 3-oxacarbacyclin and carbacyclin by the conjugate addition-azoalkene-asymmetric olefination strategy.
Kim M; Gais HJ
J Org Chem; 2006 Jun; 71(12):4642-50. PubMed ID: 16749799
[TBL] [Abstract][Full Text] [Related]
4. Asymmetric synthesis of 3-oxa-15-Deoxy-16-(m-tolyl)-17,18,19,20-tetranorisocarbacyclin and its neuroprotective analogue 15-Deoxy-16-(m-tolyl)-17,18,19,20-tetranorisocarbacyclin based on the conjugate addition-azoalkene-asymmetric olefination strategy.
van de Sande M; Gais HJ
Chemistry; 2007; 13(6):1784-95. PubMed ID: 17106906
[TBL] [Abstract][Full Text] [Related]
5. Asymmetric synthesis of the highly potent anti-metastatic prostacyclin analogue cicaprost and its isomer isocicaprost.
Lerm M; Gais HJ; Cheng K; Vermeeren C
J Am Chem Soc; 2003 Aug; 125(32):9653-67. PubMed ID: 12904032
[TBL] [Abstract][Full Text] [Related]
6. A new strategy for the enantioselective synthesis of carba-prostacyclin analogues based on organocopper conjugate addition to a bicyclic azoene and its application to the synthesis of 13,14-dinor-inter-p-phenylene carbacyclin.
van Bergen M; Gais HJ
J Am Chem Soc; 2002 Apr; 124(16):4321-8. PubMed ID: 11960461
[TBL] [Abstract][Full Text] [Related]
7. Copper(I)-catalyzed addition of Grignard reagents to in situ-derived N-sulfonyl azoalkenes: an umpolung alkylation procedure applicable to the formation of up to three contiguous quaternary centers.
Hatcher JM; Coltart DM
J Am Chem Soc; 2010 Apr; 132(13):4546-7. PubMed ID: 20232808
[TBL] [Abstract][Full Text] [Related]
8. An efficient and stereoselective synthesis of the monomeric counterpart of marinomycin A.
Amans D; Bellosta V; Cossy J
Org Lett; 2007 Apr; 9(8):1453-6. PubMed ID: 17355145
[TBL] [Abstract][Full Text] [Related]
9. Recent advances in efficient and selective synthesis of di-, tri-, and tetrasubstituted alkenes via Pd-catalyzed alkenylation-carbonyl olefination synergy.
Negishi E; Huang Z; Wang G; Mohan S; Wang C; Hattori H
Acc Chem Res; 2008 Nov; 41(11):1474-85. PubMed ID: 18783256
[TBL] [Abstract][Full Text] [Related]
10. Highly enantioselective carbon-carbon bond formation by Cu-catalyzed asymmetric [2,3]-sigmatropic rearrangement: application to the syntheses of seven-membered oxacycles and six-membered carbocycles.
Kumaraswamy G; Sadaiah K; Ramakrishna DS; Police N; Sridhar B; Bharatam J
Chem Commun (Camb); 2008 Nov; (42):5324-6. PubMed ID: 18985198
[TBL] [Abstract][Full Text] [Related]
11. A "chiral aldehyde" equivalent as a building block towards biologically active targets.
Trost BM; Crawley ML
Chemistry; 2004 May; 10(9):2237-52. PubMed ID: 15112213
[TBL] [Abstract][Full Text] [Related]
12. Toward the development of a general chiral auxiliary. Enantioselective alkylation and a new catalytic asymmetric addition of silyloxyfurans: application to a total synthesis of (-)-rasfonin.
Boeckman RK; Pero JE; Boehmler DJ
J Am Chem Soc; 2006 Aug; 128(34):11032-3. PubMed ID: 16925414
[TBL] [Abstract][Full Text] [Related]
13. Enantioselective synthesis of chiral sulfones by Rh-catalyzed asymmetric addition of boronic acids to alpha,beta-unsaturated 2-pyridyl sulfones.
Mauleón P; Alonso I; Rivero MR; Carretero JC
J Org Chem; 2007 Dec; 72(26):9924-35. PubMed ID: 18047369
[TBL] [Abstract][Full Text] [Related]
14. Nickel-catalyzed enantioselective alkylative coupling of alkynes and aldehydes: synthesis of chiral allylic alcohols with tetrasubstituted olefins.
Yang Y; Zhu SF; Zhou CY; Zhou QL
J Am Chem Soc; 2008 Oct; 130(43):14052-3. PubMed ID: 18834121
[TBL] [Abstract][Full Text] [Related]
15. Catalytic asymmetric conjugate addition and allylic alkylation with Grignard reagents.
Harutyunyan SR; den Hartog T; Geurts K; Minnaard AJ; Feringa BL
Chem Rev; 2008 Aug; 108(8):2824-52. PubMed ID: 18698733
[No Abstract] [Full Text] [Related]
16. Nickel-catalyzed asymmetric negishi cross-couplings of secondary allylic chlorides with alkylzincs.
Son S; Fu GC
J Am Chem Soc; 2008 Mar; 130(9):2756-7. PubMed ID: 18257579
[TBL] [Abstract][Full Text] [Related]
17. Highly regio- and stereoselective addition of organolithium reagents to extended conjugate amides using (S,S)-(+)-pseudoephedrine as chiral auxiliary.
Ocejo M; Carrillo L; Badía D; Vicario JL; Fernández N; Reyes E
J Org Chem; 2009 Jun; 74(11):4404-7. PubMed ID: 19402699
[TBL] [Abstract][Full Text] [Related]
18. Total synthesis of (+)-neomarinone.
Peña-López M; Martínez MM; Sarandeses LA; Pérez Sestelo J
Chemistry; 2009; 15(4):910-6. PubMed ID: 19053110
[TBL] [Abstract][Full Text] [Related]
19. Catalytic intermolecular allylic C-H alkylation.
Young AJ; White MC
J Am Chem Soc; 2008 Oct; 130(43):14090-1. PubMed ID: 18831588
[TBL] [Abstract][Full Text] [Related]
20. Synthesis of a tetrahydropyran NK1 receptor antagonist via asymmetric conjugate addition.
Huffman MA; Smitrovich JH; Rosen JD; Boice GN; Qu C; Nelson TD; McNamara JM
J Org Chem; 2005 May; 70(11):4409-13. PubMed ID: 15903319
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
