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Visible-Light-Driven CarboxyLic Amine Protocol (CLAP) for the Synthesis of 2‑Substituted Piperazines under Batch and Flow Conditions

Organic letters, 2020-07, Vol.22 (13), p.5157-5162

2020

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Total Synthesis of (+)-Oxo-tomaymycin

Organic process research & development, 2020-05, Vol.24 (5), p.762-768

2020

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Fit-for-Purpose Synthesis of an Aza-Cryptophycin Analogue as the Payload for an Antibody–Drug Conjugate

Organic process research & development, 2022-08, Vol.26 (8), p.2145-2154

2022

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Total Synthesis of an Antitumor Agent RA-VII via an Efficient Preparation of Cycloisodityrosine

Journal of organic chemistry, 1999-08, Vol.64 (17), p.6283-6296

1999

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A New Approach to the Synthesis of Piperazinomycin and Bouvardin: Facile Access to Cycloisodityrosine via an Intramolecular SNAr Reaction

Journal of organic chemistry, 1996-01, Vol.61 (2), p.771-774

1996

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4-Nitrophenyltriflate and 4-Nitrophenylnonaflate as New Perfluoroalkanesulfonyl Transfer Agents: Experimental and Computational Studies

Journal of organic chemistry, 1999-10, Vol.64 (20), p.7638-7642

1999

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Some Items of Interest to Process R&D Chemists and Engineers

Organic process research & development, 2016-06, Vol.20 (6), p.997-1007

2016

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Some Items of Interest to Process R&D Chemists and Engineers

Organic process research & development, 2016-04, Vol.20 (4), p.693-699

2016

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Some Items of Interest to Process R&D Chemists and Engineers

Organic process research & development, 2015-11, Vol.19 (11), p.1703-1710

2015

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Total Synthesis of Herbimycin A

Organic letters, 2007-01, Vol.9 (1), p.145-148

2007

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Some Items of Interest to Process R&D Chemists and Engineers

Organic process research & development, 2016-02, Vol.20 (2), p.105-122

2016

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Studies toward Diazonamide A: Initial Synthetic Forays Directed toward the Originally Proposed Structure

Journal of the American Chemical Society, 2004-08, Vol.126 (32), p.10162-10173

2004

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An easy access to functionalized diaryl ethers: Formal total synthesis of K-13

Tetrahedron letters, 1994-08, Vol.35 (31), p.5649-5652

1994

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Solution and Solid-Phase Synthesis of Functionalized 3-Arylbenzofurans by a Novel Cyclofragmentation - Release Pathway

Angewandte Chemie International Edition, 2000-03, Vol.39 (6), p.1093-1096

2000

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Rearrangement of Homoallylic Alcohols Induced by DAST

Organic letters, 2006-05, Vol.8 (10), p.2091-2094

2006

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Total Synthesis of 16-Desmethylepothilone B, Epothilone B10, Epothilone F, and Related Side Chain Modified Epothilone B Analogues

Chemistry : a European journal, 2000-08, Vol.6 (15), p.2783-2800

2000

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Reductive deprotection of aryl allyl ethers with Pd(Ph3)4/NaBH4

Tetrahedron letters, 1994-06, Vol.35 (25), p.4349-4350

1994

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An efficient total synthesis of K-13, a non-competitive inhibitor of ACE I

Tetrahedron letters, 2000-06, Vol.41 (23), p.4573-4577

2000

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Synthesis of cycloisodityrosine revisited: A selective ring forming process

Tetrahedron letters, 1998-02, Vol.39 (7), p.551-554

1998

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A formal total synthesis of deoxybouvardin

Tetrahedron, 1997-08, Vol.53 (31), p.10753-10764

1997

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A novel synthesis of K-13

Tetrahedron letters, 1994-10, Vol.35 (40), p.7391-7394

1994

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Synthesis of 16-desmethylepothilone B: improved methodology for the rapid, highly selective and convergent construction of epothilone B and analogues

Chemical communications (Cambridge, England), 1999-03 (6), p.519-520

1999

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4-Nitrophenyltriflate as a new triflating agent

Tetrahedron letters, 1997-02, Vol.38 (7), p.1181-1182

1997

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A New Approach to the Synthesis of Piperazinomycin and Bouvardin: Facile Access to Cycloisodityrosine via an Intramolecular S N Ar Reaction

Journal of organic chemistry, 1996-01, Vol.61 (2), p.771-774

1996

Volltextzugriff (PDF)

Reductive deprotection of aryl allyl ethers with Pd(Ph 3) 4/NaBH 4

Tetrahedron letters, 1994, Vol.35 (25), p.4349-4350

1994

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Visible-Light-Driven CarboxyLic Amine Protocol (CLAP) for the Synthesis of 2‑Substituted Piperazines under Batch and Flow Conditions

Total Synthesis of (+)-Oxo-tomaymycin

Fit-for-Purpose Synthesis of an Aza-Cryptophycin Analogue as the Payload for an Antibody–Drug Conjugate

Total Synthesis of an Antitumor Agent RA-VII via an Efficient Preparation of Cycloisodityrosine

A New Approach to the Synthesis of Piperazinomycin and Bouvardin: Facile Access to Cycloisodityrosine via an Intramolecular SNAr Reaction

4-Nitrophenyltriflate and 4-Nitrophenylnonaflate as New Perfluoroalkanesulfonyl Transfer Agents: Experimental and Computational Studies

Some Items of Interest to Process R&D Chemists and Engineers

Some Items of Interest to Process R&D Chemists and Engineers

Some Items of Interest to Process R&D Chemists and Engineers

Total Synthesis of Herbimycin A

Some Items of Interest to Process R&D Chemists and Engineers

Studies toward Diazonamide A: Initial Synthetic Forays Directed toward the Originally Proposed Structure

An easy access to functionalized diaryl ethers: Formal total synthesis of K-13

Solution and Solid-Phase Synthesis of Functionalized 3-Arylbenzofurans by a Novel Cyclofragmentation - Release Pathway

Rearrangement of Homoallylic Alcohols Induced by DAST

Total Synthesis of 16-Desmethylepothilone B, Epothilone B10, Epothilone F, and Related Side Chain Modified Epothilone B Analogues

Reductive deprotection of aryl allyl ethers with Pd(Ph3)4/NaBH4

An efficient total synthesis of K-13, a non-competitive inhibitor of ACE I

Synthesis of cycloisodityrosine revisited: A selective ring forming process

A formal total synthesis of deoxybouvardin

A novel synthesis of K-13

Synthesis of 16-desmethylepothilone B: improved methodology for the rapid, highly selective and convergent construction of epothilone B and analogues

4-Nitrophenyltriflate as a new triflating agent

A New Approach to the Synthesis of Piperazinomycin and Bouvardin: Facile Access to Cycloisodityrosine via an Intramolecular S N Ar Reaction

Reductive deprotection of aryl allyl ethers with Pd(Ph 3) 4/NaBH 4

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