115 related articles for article (PubMed ID: 11418038)
1. A method to accomplish a 1,4-addition reaction of bulky nucleophiles to enones and subsequent formation of reactive enolates.
William AD; Kobayashi Y
Org Lett; 2001 Jun; 3(13):2017-20. PubMed ID: 11418038
[TBL] [Abstract][Full Text] [Related]
2. Synthesis of tetrahydrocannabinols based on an indirect 1,4-addition strategy.
William AD; Kobayashi Y
J Org Chem; 2002 Dec; 67(25):8771-82. PubMed ID: 12467388
[TBL] [Abstract][Full Text] [Related]
3. Activation of Marginally Reactive Boron Enolates by MeLi for the Formation of Enol Phosphates and Synthesis of the Δ(9)-THC Intermediate.
Kawada H; Ikoma A; Ogawa N; Kobayashi Y
J Org Chem; 2015 Sep; 80(18):9192-9. PubMed ID: 26325002
[TBL] [Abstract][Full Text] [Related]
4. Palladium(II)-Catalyzed Dehydroboration via Generation of Boron Enolates.
Sakamoto Y; Amaya T; Suzuki T; Hirao T
Chemistry; 2016 Dec; 22(52):18686-18689. PubMed ID: 27734542
[TBL] [Abstract][Full Text] [Related]
5. Dihaloindium hydride as a novel reducing agent.
Baba A; Shibata I
Chem Rec; 2005; 5(6):323-35. PubMed ID: 16278827
[TBL] [Abstract][Full Text] [Related]
6. Pd(OH)2/C-mediated selective oxidation of silyl enol ethers by tert-butylhydroperoxide, a useful method for the conversion of ketones to alpha,beta-enones or beta-silyloxy-alpha,beta-enones.
Yu JQ; Wu HC; Corey EJ
Org Lett; 2005 Mar; 7(7):1415-7. PubMed ID: 15787520
[TBL] [Abstract][Full Text] [Related]
7. Enamides and enecarbamates as nucleophiles in stereoselective C-C and C-N bond-forming reactions.
Matsubara R; Kobayashi S
Acc Chem Res; 2008 Feb; 41(2):292-301. PubMed ID: 18281949
[TBL] [Abstract][Full Text] [Related]
8. A novel reaction for annulation onto alpha,beta-unsaturated ketones: W(CO)(5).L promoted exo- and endo-selective cyclizations of omega-acetylenic silyl enol ethers prepared by 1,4-addition of propargyl malonate to enones.
Iwasawa N; Maeyama K; Kusama H
Org Lett; 2001 Nov; 3(24):3871-3. PubMed ID: 11720557
[TBL] [Abstract][Full Text] [Related]
9. High chelation control of three contiguous stereogenic centers in the Reformatsky reactions of indium enolates with alpha-hydroxy ketones: unexpected stereochemistry of lactone formation.
Babu SA; Yasuda M; Okabe Y; Shibata I; Baba A
Org Lett; 2006 Jul; 8(14):3029-32. PubMed ID: 16805544
[TBL] [Abstract][Full Text] [Related]
10. Enolate generation under hydrogenation conditions: catalytic aldol cycloreduction of keto-enones.
Huddleston RR; Krische MJ
Org Lett; 2003 Apr; 5(7):1143-6. PubMed ID: 12659594
[TBL] [Abstract][Full Text] [Related]
11. Highly stereoselective aldol reactions of titanium enolates from lactate-derived chiral ketones.
Solsona JG; Romea P; Urpí F; Vilarrasa J
Org Lett; 2003 Feb; 5(4):519-22. PubMed ID: 12583758
[TBL] [Abstract][Full Text] [Related]
12. A systematic study of the effects of relative configuration, protecting group, and enolate type on the diastereoselectivities of aldol reactions of a chiral ethyl ketone with 2-methylpropanal.
Ward DE; Kundu D; Biniaz M; Jana S
J Org Chem; 2014 Aug; 79(15):6868-94. PubMed ID: 25029195
[TBL] [Abstract][Full Text] [Related]
13. Highly stereoselective three-component reactions of phenylselenomagnesium bromide, acetylenic sulfones, and saturated aldehydes/ketones or alpha,beta-unsaturated enals or enones.
Huang X; Xie M
J Org Chem; 2002 Dec; 67(25):8895-900. PubMed ID: 12467405
[TBL] [Abstract][Full Text] [Related]
14. One-pot three-component reaction for the synthesis of alpha-(aminoethyl)-alpha,beta-enones.
Bertozzi F; Gustafsson M; Olsson R
Org Lett; 2002 Nov; 4(24):4333-6. PubMed ID: 12443091
[TBL] [Abstract][Full Text] [Related]
15. Iodotrimethylsilane-Promoted 1,4-Addition of Copper Acetylides to alpha,beta-Unsaturated Ketones and Aldehydes.
Eriksson M; Iliefski T; Nilsson M; Olsson T
J Org Chem; 1997 Jan; 62(1):182-187. PubMed ID: 11671379
[TBL] [Abstract][Full Text] [Related]
16. Studies on K2CO3-catalyzed 1,4-addition of 1,2-allenic ketones with diethyl malonate: controlled selective synthesis of beta,gamma-unsaturated enones and alpha-pyrones.
Ma S; Yu S; Yin S
J Org Chem; 2003 Nov; 68(23):8996-9002. PubMed ID: 14604373
[TBL] [Abstract][Full Text] [Related]
17. P(PhCH2NCH2CH2)3N catalysis of Mukaiyama aldol reactions of aliphatic, aromatic, and heterocyclic aldehydes and trifluoromethyl phenyl ketone.
Chintareddy VR; Wadhwa K; Verkade JG
J Org Chem; 2009 Nov; 74(21):8118-32. PubMed ID: 19795856
[TBL] [Abstract][Full Text] [Related]
18. Tandem asymmetric conjugate addition--silylation of enantiomerically enriched zinc enolates. Synthetic importance and mechanistic implications.
Knopff O; Alexakis A
Org Lett; 2002 Oct; 4(22):3835-7. PubMed ID: 12599471
[TBL] [Abstract][Full Text] [Related]
19. Catalytic addition of metallo-aldehyde enolates to ketones: a new C-C bond-forming hydrogenation.
Koech PK; Krische MJ
Org Lett; 2004 Mar; 6(5):691-4. PubMed ID: 14986951
[TBL] [Abstract][Full Text] [Related]
20. Synthesis of β-Amino-Substituted Enones by Addition of Substituted Methyl Enones to Sulfinimines: Application to the Total Synthesis of Alkaloids (+)-Lasubine II and (+)-241D and the Formal Total Synthesis of (-)-Lasubine I.
Reddy AA; Reddy PO; Prasad KR
J Org Chem; 2016 Nov; 81(22):11363-11371. PubMed ID: 27732001
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
