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Microwave‐enhanced enzyme reaction for protein mapping by mass spectrometry: A new approach to protein digestion in minutes

Protein science, 2002-11, Vol.11 (11), p.2676-2687

2002

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A simplified green chemistry approach to the Biginelli reaction using ‘Grindstone Chemistry’

Tetrahedron letters, 2004-11, Vol.45 (45), p.8351-8353

2004

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Microwave initiated reactions: Pechmann coumarin synthesis, Biginelli reaction, and acylation

Tetrahedron letters, 2006-04, Vol.47 (14), p.2423-2425

2006

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Microwave-induced organic reaction enhancement chemistry. 2. Simplified techniques

Journal of organic chemistry, 1991-12, Vol.56 (25), p.6968-6970

1991

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MORE Chemistry for Less Pollution: Applications for Process Development

Synthesis (Stuttgart), 2002, Vol.2002 (11), p.1578-1591

2002

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A Facile Iodine-catalyzed Glycosylation: Enantiomerically Pure β-Lactams with the Thienamycin Side Chain

Heterocycles, 2009-10, Vol.78 (10), p.2443

2009

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Polyhydroxy Amino Acid Derivatives via β-Lactams Using Enantiospecific Approaches and Microwave Techniques

Tetrahedron, 2000-07, Vol.56 (31), p.5603-5619

2000

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Chemoenzymatic preparation of intermediates for the taxol side chain and analogs

Molecular medicine reports, 2010-03, Vol.3 (2), p.317-318

2010

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Vinyl-β-lactams as Efficient Synthons. Eco-friendly Approaches via Microwave Assisted Reactions

Tetrahedron, 2000-07, Vol.56 (31), p.5587-5601

2000

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Chemoenzymatic preparation of intermediates for the taxol side chain and analogs

Molecular medicine reports, 2010-03, Vol.3 (2), p.317

2010

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Microwave-Assisted Rapid and Simplified Hydrogenation1

Journal of organic chemistry, 1999-08, Vol.64 (16), p.5746-5753

1999

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Microwave enhanced Akabori reaction for peptide analysis

Journal of the American Society for Mass Spectrometry, 2002-07, Vol.13 (7), p.839-850

2002

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Stereospecific Glycosylation via Ferrier Rearrangement for Optical Resolution

Journal of organic chemistry, 1994-08, Vol.59 (17), p.4714-4716

1994

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Microwave-assisted rapid synthesis of α-amino-β-lactams

Tetrahedron letters, 1996-09, Vol.37 (39), p.6989-6992

1996

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Microwave enhanced greener synthesis of indazoles via nitrenes

Tetrahedron letters, 2006-09, Vol.47 (38), p.6795-6797

2006

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Synthesis and Conformational Studies on 3- o -Tolylhydantoins by NMR and Molecular Modeling: Dipole-π Attractions in Peptides and Proteins

Bulletin of the Chemical Society of Japan, 2001-10, Vol.74 (10), p.1917-1925

2001

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Studies on lactams. 89. Versatile .beta.-lactam synthons: enantiospecific synthesis of (-)-polyoxamic acid

Journal of organic chemistry, 1993-01, Vol.58 (2), p.307-309

1993

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Studies on Substituted Beta Lactams Towards Ring Opening: Elimination Versus Rearrangement

Modern chemistry & applications, 2018, Vol.6 (2)

2018

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Molecular Ion Enhancement Using Salts in FAB Matrices for Studies on Complex Natural Products

Journal of natural products (Washington, D.C.), 1989-05, Vol.52 (3), p.534-546

1989

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Large scale Biginelli reaction via water-based biphasic media: a green chemistry strategy

Tetrahedron letters, 2005-03, Vol.46 (11), p.1901-1903

2005

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Microwave promoted energy-efficient N-formylation with aqueous formic acid

Tetrahedron letters, 2006-07, Vol.47 (27), p.4605-4607

2006

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Studies on lactams. 81. Enantiospecific synthesis and absolute configuration of substituted .beta.-lactams from D-glyceraldehyde acetonide

Journal of organic chemistry, 1988-09, Vol.53 (18), p.4227-4236

1988

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Conversion of beta-lactams to versatile synthons via molecular rearrangement and lactam cleavage

Heterocycles, 1988, Vol.27 (7), p.1755-1802

1988

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Stereoselective chiral synthesis of N-aryl-.alpha.-amino-.beta.-lactams from .beta.-hydroxy-.alpha.-amino acids

Journal of organic chemistry, 1981-03, Vol.46 (6), p.1229-1230

1981

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Microwave-induced, Montmorillonite K10-catalyzed Ferrier rearrangement of tri- O-acetyl- d-galactal: mild, eco-friendly, rapid glycosidation with allylic rearrangement

Tetrahedron letters, 2002-09, Vol.43 (38), p.6795-6798

2002

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Microwave‐enhanced enzyme reaction for protein mapping by mass spectrometry: A new approach to protein digestion in minutes

A simplified green chemistry approach to the Biginelli reaction using ‘Grindstone Chemistry’

Microwave initiated reactions: Pechmann coumarin synthesis, Biginelli reaction, and acylation

Microwave-induced organic reaction enhancement chemistry. 2. Simplified techniques

MORE Chemistry for Less Pollution: Applications for Process Development

A Facile Iodine-catalyzed Glycosylation: Enantiomerically Pure β-Lactams with the Thienamycin Side Chain

Polyhydroxy Amino Acid Derivatives via β-Lactams Using Enantiospecific Approaches and Microwave Techniques

Chemoenzymatic preparation of intermediates for the taxol side chain and analogs

Vinyl-β-lactams as Efficient Synthons. Eco-friendly Approaches via Microwave Assisted Reactions

Chemoenzymatic preparation of intermediates for the taxol side chain and analogs

Microwave-Assisted Rapid and Simplified Hydrogenation1

Microwave enhanced Akabori reaction for peptide analysis

Stereospecific Glycosylation via Ferrier Rearrangement for Optical Resolution

Microwave-assisted rapid synthesis of α-amino-β-lactams

Microwave enhanced greener synthesis of indazoles via nitrenes

Synthesis and Conformational Studies on 3- o -Tolylhydantoins by NMR and Molecular Modeling: Dipole-π Attractions in Peptides and Proteins

Studies on lactams. 89. Versatile .beta.-lactam synthons: enantiospecific synthesis of (-)-polyoxamic acid

Studies on Substituted Beta Lactams Towards Ring Opening: Elimination Versus Rearrangement

Molecular Ion Enhancement Using Salts in FAB Matrices for Studies on Complex Natural Products

Large scale Biginelli reaction via water-based biphasic media: a green chemistry strategy

Microwave promoted energy-efficient N-formylation with aqueous formic acid

Studies on lactams. 81. Enantiospecific synthesis and absolute configuration of substituted .beta.-lactams from D-glyceraldehyde acetonide

Conversion of beta-lactams to versatile synthons via molecular rearrangement and lactam cleavage

Stereoselective chiral synthesis of N-aryl-.alpha.-amino-.beta.-lactams from .beta.-hydroxy-.alpha.-amino acids

Microwave-induced, Montmorillonite K10-catalyzed Ferrier rearrangement of tri- O-acetyl- d-galactal: mild, eco-friendly, rapid glycosidation with allylic rearrangement

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