메뉴 건너뛰기




Volumn 13, Issue 2, 2008, Pages 331-339

A facile route to diastereomeric phosphorus ylides. Chemoselective synthesis of dialkyl (E)-2-[1-(2-oxocyclopentylidene)ethyl]-2-butenedioates

Author keywords

2 acetylcyclopentanone; Intramolecular wittig reaction; Phosphorus ylides; Spirocompounds

Indexed keywords

ALKENE; HYDROCARBON; PHOSPHORUS;

EID: 40349088951     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules13020331     Document Type: Article
Times cited : (9)

References (23)
  • 2
    • 0000114788 scopus 로고    scopus 로고
    • New Synthetic Methodologies for Carbon-Carbon Double Bond Formation
    • Shen, Y. New Synthetic Methodologies for Carbon-Carbon Double Bond Formation. Acc. Chem Re. 1998, 31, 584-592.
    • (1998) Acc. Chem Re , vol.31 , pp. 584-592
    • Shen, Y.1
  • 3
    • 0000775741 scopus 로고    scopus 로고
    • Evidence for a Continuous Transition between Thiaphosphetane and Betaine-Type Structures in the Thio-Wittig Reaction
    • Puke, C.; Erker, G.; Aust, N. C.; Wurthwein, E. V.; Frohlich, R. Evidence for a Continuous Transition between Thiaphosphetane and Betaine-Type Structures in the Thio-Wittig Reaction. J. Am. Chem. Soc. 1998, 120, 4863-4864.
    • (1998) J. Am. Chem. Soc , vol.120 , pp. 4863-4864
    • Puke, C.1    Erker, G.2    Aust, N.C.3    Wurthwein, E.V.4    Frohlich, R.5
  • 5
    • 40349115682 scopus 로고    scopus 로고
    • pp. 42-47;
    • a) pp. 42-47;
  • 6
    • 40349114010 scopus 로고    scopus 로고
    • pp. 319-323;
    • b) pp. 319-323;
  • 7
    • 40349092588 scopus 로고    scopus 로고
    • pp. 361-362
    • c) pp. 361-362.
  • 10
    • 40349097513 scopus 로고    scopus 로고
    • p. 166;
    • a) p. 166;
  • 11
    • 40349083479 scopus 로고    scopus 로고
    • p. 174;
    • b) p. 174;
  • 12
    • 40349114011 scopus 로고    scopus 로고
    • p. 179;
    • c) p. 179;
  • 13
    • 40349099772 scopus 로고    scopus 로고
    • p. 199
    • d) p. 199.
  • 14
    • 0001848341 scopus 로고
    • The Wittig olefination reaction and modifications involving phosphoryl stabilized carbanions. Stereochemistry, mechanism and selected synthetic aspects
    • Maryanoff, B. G.; Reitz, A. B. The Wittig olefination reaction and modifications involving phosphoryl stabilized carbanions. Stereochemistry, mechanism and selected synthetic aspects. Chem. Rev. 1989, 89, 863-927.
    • (1989) Chem. Rev , vol.89 , pp. 863-927
    • Maryanoff, B.G.1    Reitz, A.B.2
  • 15
    • 0001154962 scopus 로고    scopus 로고
    • Methods of Preparation of C-Substituted Phosphorus Ylides and their Application in Organic Synthesis
    • Kolodiazhynyi, O. I. Methods of Preparation of C-Substituted Phosphorus Ylides and their Application in Organic Synthesis. Russ. Chem. Rev. 1997, 66, 225-254.
    • (1997) Russ. Chem. Rev , vol.66 , pp. 225-254
    • Kolodiazhynyi, O.I.1
  • 16
    • 0000480968 scopus 로고
    • Low- Coordinate Hyper Valent Phosphorus
    • Arduago, A. J.; Stewart, C. A. Low- Coordinate Hyper Valent Phosphorus. Chem. Rev. 1994, 94, 1215-1237.
    • (1994) Chem. Rev , vol.94 , pp. 1215-1237
    • Arduago, A.J.1    Stewart, C.A.2
  • 17
    • 0033214022 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Highly Functionalized Cyclobutenes. A Facile Rout to Electron-Deficient 1,3-Dienes
    • Yavari, I.; Asghari, S. Stereoselective Synthesis of Highly Functionalized Cyclobutenes. A Facile Rout to Electron-Deficient 1,3-Dienes. Tetrahedron 1999, 55, 11853-11858.
    • (1999) Tetrahedron , vol.55 , pp. 11853-11858
    • Yavari, I.1    Asghari, S.2
  • 18
    • 0033036302 scopus 로고    scopus 로고
    • Vinyltriphenylphosphonium Salt-mediated New Synthesis of Functionalized Maleimides
    • Yavari, I.; Asghari S.; Esmaili, A. A. Vinyltriphenylphosphonium Salt-mediated New Synthesis of Functionalized Maleimides. J. Chem. Res. 1999, 234-235.
    • (1999) J. Chem. Res , pp. 234-235
    • Yavari, I.1    Asghari, S.2    Esmaili, A.A.3
  • 19
    • 0032568045 scopus 로고    scopus 로고
    • New One-pot Synthesis of tetra- Alkoxycarbonylallylidenetriphenylphosphoranes
    • Yavari, I.; Baharfar, R. New One-pot Synthesis of tetra- Alkoxycarbonylallylidenetriphenylphosphoranes. Tetrahedron Lett. 1998, 39, 1051-1054.
    • (1998) Tetrahedron Lett , vol.39 , pp. 1051-1054
    • Yavari, I.1    Baharfar, R.2
  • 20
    • 0037090235 scopus 로고    scopus 로고
    • Yavari, I.; Adib, M.; Sayahi, M. H. An efficient diastereoselective one-pot synthesis of dihydrofuro[2′,3′: 2,3]indeno[2,1-b]furan derivatives. Tetrahedron Lett. 2002, 43, 2927-2929.
    • Yavari, I.; Adib, M.; Sayahi, M. H. An efficient diastereoselective one-pot synthesis of dihydrofuro[2′,3′: 2,3]indeno[2,1-b]furan derivatives. Tetrahedron Lett. 2002, 43, 2927-2929.
  • 21
    • 33847143193 scopus 로고    scopus 로고
    • 3P with activated acetylenes in the presence of dimethyl methoxymalonate
    • 3P with activated acetylenes in the presence of dimethyl methoxymalonate. Phosphorus, Sulfur, Silicon Rel. Elem., 2007, 182, 595-600.
    • (2007) Phosphorus, Sulfur, Silicon Rel. Elem , vol.182 , pp. 595-600
    • Yavari, I.1    Karimi, E.2
  • 22
    • 30744477447 scopus 로고    scopus 로고
    • Three component reaction between triphenylphosphine, dialkyl acetylenedicarboxylates and urea or N-methyl urea
    • Yavari, I.; Zabarjad-Shiraz, N. Three component reaction between triphenylphosphine, dialkyl acetylenedicarboxylates and urea or N-methyl urea. Mol. Div. 2006, 10, 23-27.
    • (2006) Mol. Div , vol.10 , pp. 23-27
    • Yavari, I.1    Zabarjad-Shiraz, N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.