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Formal Synthesis of (+)-Discodermolide

Organic letters, 2003-04, Vol.5 (8), p.1233-1236

2003

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Proteomics-based target identification: bengamides as a new class of methionine aminopeptidase inhibitors

The Journal of biological chemistry, 2003-12, Vol.278 (52), p.52964-52971

2003

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Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 1: Synthetic Strategy and Preparation of a Common Precursor

Organic process research & development, 2004-01, Vol.8 (1), p.92-100

2004

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Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 4: Preparation of Fragment C7 - 24

Organic process research & development, 2004-01, Vol.8 (1), p.113-121

2004

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Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 3: Synthesis of Fragment C15 - 21

Organic process research & development, 2004-01, Vol.8 (1), p.107-112

2004

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Synthesis and Antitumor Activity of Ester-Modified Analogues of Bengamide B

Journal of medicinal chemistry, 2001-10, Vol.44 (22), p.3692-3699

2001

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Total Syntheses of Bengamides B and E

Journal of organic chemistry, 2001-03, Vol.66 (6), p.2118-2122

2001

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Rhodium(II)-catalyzed cyclization of 2-alkynyl 2-diazo-3-oxobutanoates as a method for synthesizing substituted furans

Journal of organic chemistry, 1993-01, Vol.58 (1), p.21-28

1993

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Proteomics-based Target Identification

The Journal of biological chemistry, 2003-12, Vol.278 (52), p.52964-52971

2003

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Design, synthesis, and antitumor activity of bicyclic and isomeric analogues of illudin M

Bioorganic & medicinal chemistry letters, 1996-05, Vol.6 (9), p.1029-1034

1996

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Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 5: Linkage of Fragments C1 - 6 and C7 - 24 and Finale

Organic process research & development, 2004-01, Vol.8 (1), p.122-130

2004

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Bengamides Revisited: New Structures and Antitumor Studies

Journal of organic chemistry, 2001-03, Vol.66 (5), p.1733-1741

2001

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Synthesis of 3-pyrrolines by an intramolecular Wittig reaction

Journal of organic chemistry, 1991-10, Vol.56 (22), p.6475-6477

1991

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SYNTHETIC APPROACHES TOWARD THE BENGAMIDE FAMILY OF ANTITUMOR MARINE NATURAL PRODUCTS. A REVIEW

Organic preparations and procedures international, 2002-12, Vol.34 (6), p.559-583

Kinder, Frederick R.

2002

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Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 2: Synthesis of Fragments C1 - 6 and C9-14

Organic process research & development, 2004-01, Vol.8 (1), p.101-106

2004

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Total Synthesis of (.+-.)-Illudin M

Journal of organic chemistry, 1994-11, Vol.59 (23), p.6965-6967

1994

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Synthesis of 3,9b-dihydro-5H-pyrrolo[2,1-a]isoindoles and 3,5,6,10b-tetrahydropyrrolo[2,1-a]isoquinolines with 1,3-dipolar cycloaddition reactions

Journal of heterocyclic chemistry, 1990-05, Vol.27 (4), p.975-979

1990

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Structure, synthesis, and antitumor activity of the hydrolysis product of the antitumor agent carmethizole

Drug development research, 1993-11, Vol.30 (3), p.143-146

1993

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Preparation of oxygenated heterocycles via the cyclization reaction of α-diazo substituted alkynes

Tetrahedron letters, 1990, Vol.31 (47), p.6835-6838

1990

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Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 3: Synthesis of Fragment C 15 - 21

Organic process research & development, 2004-01, Vol.8 (1), p.107-112

2004

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Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 5: Linkage of Fragments C 1 - 6 and C 7 - 24 and Finale

Organic process research & development, 2004-01, Vol.8 (1), p.122-130

2004

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Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 2: Synthesis of Fragments C 1 - 6 and C 9-14

Organic process research & development, 2004-01, Vol.8 (1), p.101-106

2004

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Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 4: Preparation of Fragment C 7 - 24

Organic process research & development, 2004-01, Vol.8 (1), p.113-121

2004

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Synthetic Approaches Toward the Bengamide Family of Antitumor Marine Natural Products

ChemInform, 2003-04, Vol.34 (16), p.no-no

Kinder, Frederick R. Jr

2003

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Synthesis of Isodehydroilludin M

Synthetic communications, 1998-07, Vol.28 (13), p.2541-2548

1998

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Formal Synthesis of (+)-Discodermolide

Proteomics-based target identification: bengamides as a new class of methionine aminopeptidase inhibitors

Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 1: Synthetic Strategy and Preparation of a Common Precursor

Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 4: Preparation of Fragment C7 - 24

Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 3: Synthesis of Fragment C15 - 21

Synthesis and Antitumor Activity of Ester-Modified Analogues of Bengamide B

Total Syntheses of Bengamides B and E

Rhodium(II)-catalyzed cyclization of 2-alkynyl 2-diazo-3-oxobutanoates as a method for synthesizing substituted furans

Proteomics-based Target Identification

Design, synthesis, and antitumor activity of bicyclic and isomeric analogues of illudin M

Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 5: Linkage of Fragments C1 - 6 and C7 - 24 and Finale

Bengamides Revisited: New Structures and Antitumor Studies

Synthesis of 3-pyrrolines by an intramolecular Wittig reaction

SYNTHETIC APPROACHES TOWARD THE BENGAMIDE FAMILY OF ANTITUMOR MARINE NATURAL PRODUCTS. A REVIEW

Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 2: Synthesis of Fragments C1 - 6 and C9-14

Total Synthesis of (.+-.)-Illudin M

Synthesis of 3,9b-dihydro-5H-pyrrolo[2,1-a]isoindoles and 3,5,6,10b-tetrahydropyrrolo[2,1-a]isoquinolines with 1,3-dipolar cycloaddition reactions

Structure, synthesis, and antitumor activity of the hydrolysis product of the antitumor agent carmethizole

Preparation of oxygenated heterocycles via the cyclization reaction of α-diazo substituted alkynes

Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 3: Synthesis of Fragment C 15 - 21

Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 5: Linkage of Fragments C 1 - 6 and C 7 - 24 and Finale

Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 2: Synthesis of Fragments C 1 - 6 and C 9-14

Large-Scale Synthesis of the Anti-Cancer Marine Natural Product (+)-Discodermolide. Part 4: Preparation of Fragment C 7 - 24

Synthetic Approaches Toward the Bengamide Family of Antitumor Marine Natural Products

Synthesis of Isodehydroilludin M

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