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Academic Journal

Triarylaminium Radical Cation Promoted Coupling of Catharanthine with Vindoline: Diastereospecific Synthesis of Anhydrovinblastine and Reaction Scope.

  • Authors : Boon BA; Department of Chemistry and The Skaggs Institute of Chemical Biology , Scripps Research Institute , 10550 North Torrey Pines Road , La Jolla , California 92037 , United States.; Boger DL

Subjects: Amines/Amines/Amines/*chemistry ; Vinblastine/Vinblastine/Vinblastine/*analogs & derivatives ; Vinblastine/Vinblastine/Vinblastine/*chemical synthesis

  • Source: Journal of the American Chemical Society [J Am Chem Soc] 2019 Sep 11; Vol. 141 (36), pp. 14349-14355. Date of Electronic Publication: 2019 Sep 03.Publisher: American Chemical Society Country of Publication: United States NLM ID: 7503056 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Synthesis of a Potent Vinblastine: Rationally Designed Added Benign Complexity.

  • Authors : Allemann O; Department of Chemistry and the Skaggs Institute for Chemical Biology, The Scripps Research Institute , 10550 North Torrey Pines Road, La Jolla, California 92037, United States.; Brutsch M

Subjects: Drug Design*; Vinblastine/Vinblastine/Vinblastine/*chemical synthesis ; Vinblastine/Vinblastine/Vinblastine/*chemistry

  • Source: Journal of the American Chemical Society [J Am Chem Soc] 2016 Jul 13; Vol. 138 (27), pp. 8376-9. Date of Electronic Publication: 2016 Jul 01.Publisher: American Chemical Society Country of Publication: United States NLM ID: 7503056 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Total synthesis and evaluation of a key series of C5-substituted vinblastine derivatives.

  • Authors : Va P; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.; Campbell EL

Subjects: Antineoplastic Agents/Antineoplastic Agents/Antineoplastic Agents/*chemical synthesis ; Antineoplastic Agents/Antineoplastic Agents/Antineoplastic Agents/*pharmacology ; Vinblastine/Vinblastine/Vinblastine/*chemical synthesis

  • Source: Journal of the American Chemical Society [J Am Chem Soc] 2010 Jun 23; Vol. 132 (24), pp. 8489-95.Publisher: American Chemical Society Country of Publication: United States NLM ID: 7503056 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Total synthesis of vinblastine, vincristine, related natural products, and key structural analogues.

  • Authors : Ishikawa H; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.; Colby DA

Subjects: Vinblastine/Vinblastine/Vinblastine/*analogs & derivatives ; Vinblastine/Vinblastine/Vinblastine/*chemical synthesis ; Vincristine/Vincristine/Vincristine/*analogs & derivatives

  • Source: Journal of the American Chemical Society [J Am Chem Soc] 2009 Apr 08; Vol. 131 (13), pp. 4904-16.Publisher: American Chemical Society Country of Publication: United States NLM ID: 7503056 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Asymmetric total synthesis of vindorosine, vindoline, and key vinblastine analogues.

  • Authors : Sasaki Y; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.; Kato D

Subjects: Vinblastine/Vinblastine/Vinblastine/*analogs & derivatives ; Vinblastine/Vinblastine/Vinblastine/*chemical synthesis; Stereoisomerism

  • Source: Journal of the American Chemical Society [J Am Chem Soc] 2010 Sep 29; Vol. 132 (38), pp. 13533-44.Publisher: American Chemical Society Country of Publication: United States NLM ID: 7503056 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Direct coupling of catharanthine and vindoline to provide vinblastine: total synthesis of (+)- and ent-(-)-vinblastine.

  • Authors : Ishikawa H; Department of Chemistry and Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.; Colby DA

Subjects: Antineoplastic Agents, Phytogenic/Antineoplastic Agents, Phytogenic/Antineoplastic Agents, Phytogenic/*chemical synthesis ; Vinblastine/Vinblastine/Vinblastine/*analogs & derivatives ; Vinblastine/Vinblastine/Vinblastine/*chemical synthesis

  • Source: Journal of the American Chemical Society [J Am Chem Soc] 2008 Jan 16; Vol. 130 (2), pp. 420-1.Publisher: American Chemical Society Country of Publication: United States NLM ID: 7503056 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

New insights into the mechanism and an expanded scope of the Fe(III)-mediated vinblastine coupling reaction.

  • Authors : Gotoh H; Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.; Sears JE

Subjects: Ferric Compounds/Ferric Compounds/Ferric Compounds/*chemistry ; Vinblastine/Vinblastine/Vinblastine/*chemistry; Molecular Structure

  • Source: Journal of the American Chemical Society [J Am Chem Soc] 2012 Aug 15; Vol. 134 (32), pp. 13240-3. Date of Electronic Publication: 2012 Aug 07.Publisher: American Chemical Society Country of Publication: United States NLM ID: 7503056 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Stereocontrolled total synthesis of (+)-vinblastine.

  • Authors : Yokoshima S; Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.; Ueda T

Subjects: Antineoplastic Agents, Phytogenic/Antineoplastic Agents, Phytogenic/Antineoplastic Agents, Phytogenic/*chemical synthesis ; Vinblastine/Vinblastine/Vinblastine/*chemical synthesis; Catharanthus/Catharanthus/Catharanthus/chemistry

  • Source: Journal of the American Chemical Society [J Am Chem Soc] 2002 Mar 13; Vol. 124 (10), pp. 2137-9.Publisher: American Chemical Society Country of Publication: United States NLM ID: 7503056 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Asymmetric total synthesis of vindoline.

  • Authors : Kato D; Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.; Sasaki Y

Subjects: Vinblastine/Vinblastine/Vinblastine/*analogs & derivatives; Biological Products/Biological Products/Biological Products/chemical synthesis ; Biological Products/Biological Products/Biological Products/chemistry

  • Source: Journal of the American Chemical Society [J Am Chem Soc] 2010 Mar 24; Vol. 132 (11), pp. 3685-7.Publisher: American Chemical Society Country of Publication: United States NLM ID: 7503056 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Total synthesis of (-)- and ent-(+)-vindoline and related alkaloids.

  • Authors : Ishikawa H; Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.; Elliott GI

Subjects: Alkaloids/Alkaloids/Alkaloids/*chemical synthesis ; Vinblastine/Vinblastine/Vinblastine/*analogs & derivatives; Alkaloids/Alkaloids/Alkaloids/chemistry

  • Source: Journal of the American Chemical Society [J Am Chem Soc] 2006 Aug 16; Vol. 128 (32), pp. 10596-612.Publisher: American Chemical Society Country of Publication: United States NLM ID: 7503056 Publication Model: Print Cited Medium: Print ISSN:

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