254 related articles for article (PubMed ID: 18763795)
1. A two-directional approach to enantiopure 1,4-difluoro-cyclohexenes: synthesis of difluorinated cyclitol analogues.
Purser S; Claridge TD; Odell B; Moore PR; Gouverneur V
Org Lett; 2008 Oct; 10(19):4263-6. PubMed ID: 18763795
[TBL] [Abstract][Full Text] [Related]
2. Chemoenzymatic synthesis of inositols, conduritols, and cyclitol analogues.
Duchek J; Adams DR; Hudlicky T
Chem Rev; 2011 Jul; 111(7):4223-58. PubMed ID: 21630704
[No Abstract] [Full Text] [Related]
3. Sequential desymmetrization-fluorination: enantioselective synthesis of fluorinated cyclitols.
Purser S; Odell B; Claridge TD; Moore PR; Gouverneur V
Chemistry; 2006 Dec; 12(36):9176-85. PubMed ID: 17066392
[TBL] [Abstract][Full Text] [Related]
4. Construction of Optically Active Isotwistanes and Aminocyclitols Using Chiral Cyclohexadiene as a Common Intermediate.
Harada S; Li K; Kino R; Takeda T; Wu CH; Hiraoka S; Nishida A
Chem Pharm Bull (Tokyo); 2016 Oct; 64(10):1474-1483. PubMed ID: 27452927
[TBL] [Abstract][Full Text] [Related]
5. Diastereoselective synthesis of fluorinated, seven-membered beta-amino acid derivatives via ring-closing metathesis.
Fustero S; Bartolomé A; Sanz-Cervera JF; Sánchez-Roselló M; arcía Soler J; Ramírez de Arellano C; Fuentes AS
Org Lett; 2003 Jul; 5(14):2523-6. PubMed ID: 12841771
[TBL] [Abstract][Full Text] [Related]
6. Ring-closing metathesis-based synthesis of (3R,4R,5S)-4-acetylamino-5-amino-3-hydroxy- cyclohex-1-ene-carboxylic acid ethyl ester: a functionalized cycloalkene skeleton of GS4104.
Cong X; Yao ZJ
J Org Chem; 2006 Jul; 71(14):5365-8. PubMed ID: 16808528
[TBL] [Abstract][Full Text] [Related]
7. Stereodivergent syntheses of conduramines and aminocyclitols.
Alegret C; Benet-Buchholz J; Riera A
Org Lett; 2006 Jul; 8(14):3069-72. PubMed ID: 16805554
[TBL] [Abstract][Full Text] [Related]
8. A flexible strategy based on a C2-symmetric pool of chiral substrates: concise synthesis of (+)-valienamine, key intermediate of (+)- pancratistatin, and conduramines A-1 and E.
Chang YK; Lo HJ; Yan TH
Org Lett; 2009 Oct; 11(19):4278-81. PubMed ID: 19711969
[TBL] [Abstract][Full Text] [Related]
9. Synthesis and biological evaluation of new bicyclic fluorinated uracils through ring-closing metathesis.
Fustero S; Catalan S; Piera J; Sanz-Cervera JF; Fernandez B; Aceña JL
J Org Chem; 2006 May; 71(10):4010-3. PubMed ID: 16674087
[TBL] [Abstract][Full Text] [Related]
10. Synthesis of pentahydroxy indolizidine alkaloids using ring closing metathesis: attempts to find the correct structure of uniflorine A.
Karanjule NS; Markad SD; Dhavale DD
J Org Chem; 2006 Aug; 71(16):6273-6. PubMed ID: 16872219
[TBL] [Abstract][Full Text] [Related]
11. Fluorination-free synthesis of a 4,4-difluoro-3,3-dimethylproline derivative.
Chen L; Kim YM; Kucera DJ; Harrison KE; Bahmanyar S; Scott JM; Yazbeck D
J Org Chem; 2006 Jul; 71(15):5468-73. PubMed ID: 16839124
[TBL] [Abstract][Full Text] [Related]
12. Regiodivergent addition of phenols to allylic oxides: control of 1,2- and 1,4-additions for cyclitol synthesis.
Moschitto MJ; Vaccarello DN; Lewis CA
Angew Chem Int Ed Engl; 2015 Feb; 54(7):2142-5. PubMed ID: 25533617
[TBL] [Abstract][Full Text] [Related]
13. Stereoselective total synthesis of (-)-perrottetinene and assignment of its absolute configuration.
Song Y; Hwang S; Gong P; Kim D; Kim S
Org Lett; 2008 Jan; 10(2):269-71. PubMed ID: 18085788
[TBL] [Abstract][Full Text] [Related]
14. A convenient synthesis of orthogonally protected 2-deoxystreptamine (2-DOS) as an aminocyclitol scaffold for the development of novel aminoglycoside antibiotic derivatives against bacterial resistance.
Bauder C
Org Biomol Chem; 2008 Aug; 6(16):2952-60. PubMed ID: 18688488
[TBL] [Abstract][Full Text] [Related]
15. Transforming terpene feedstock into polyketide architecture.
Winter P; Vaxelaire C; Heinz C; Christmann M
Chem Commun (Camb); 2011 Jan; 47(1):394-6. PubMed ID: 20835423
[TBL] [Abstract][Full Text] [Related]
16. Stereoselective synthesis of deuterated β-cyclohexenylserine, a biosynthetic intermediate of the salinosporamides.
Deska J; Hähn S; Kazmaier U
Org Lett; 2011 Jun; 13(12):3210-3. PubMed ID: 21615116
[TBL] [Abstract][Full Text] [Related]
17. Asymmetric tandem Michael addition-ylide olefination reaction for the synthesis of optically active cyclohexa-1,3-diene derivatives.
Ye LW; Wang SB; Wang QG; Sun XL; Tang Y; Zhou YG
Chem Commun (Camb); 2009 Jun; (21):3092-4. PubMed ID: 19462097
[TBL] [Abstract][Full Text] [Related]
18. Asymmetric synthesis of new beta,beta-difluorinated cyclic quaternary alpha-amino acid derivatives.
Fustero S; Sanchez-Roselló M; Rodrigo V; del Pozo C; Sanz-Cervera JF; Simón A; Ramírez de Arellano C
Org Lett; 2006 Aug; 8(18):4129-32. PubMed ID: 16928091
[TBL] [Abstract][Full Text] [Related]
19. An efficient synthesis of valienamine via ring-closing metathesis.
Chang YK; Lee BY; Kim DJ; Lee GS; Jeon HB; Kim KS
J Org Chem; 2005 Apr; 70(8):3299-302. PubMed ID: 15823000
[TBL] [Abstract][Full Text] [Related]
20. Asymmetric synthesis of both enantiomers of point-difluorinated-eldanolide, analogues of insect sex pheromone.
Itoh T; Kudo K; Tanaka N; Zagatti P; Renou M
Enantiomer; 2001; 6(1):43-9. PubMed ID: 11434540
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]