Mechanism-based inhibition of 5-aminolaevulinic acid dehydratase from Bacillus subtilis by the 3-thia analogue of the substrate
Chemical Communications
(1996)
303
(doi: 10.1039/cc9960000303)
Stereochemical studies on the proposed spiro intermediate for the biosynthesis of the natural porphyrins: determination by a novel X-ray method of the absolute configuration of the spirolactam which inhibits cosynthetase
Chemical Communications
(1995)
1789
(doi: 10.1039/c39950001789)
Stereocontrolled syntheses of polyhydroxy indolizidines, including 8a-epi-, 6,8a-diepi- and 1,6-diepi-castanospermine, starting from malic acid
Tetrahedron Letters
(1995)
36
2335
(doi: 10.1016/0040-4039(95)00249-C)
Bridged thiazolium salts as models for thiamin: NMR, crystallographic and molecular mechanics studies
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
(1995)
777
(doi: 10.1039/p29950000777)
Biosynthesis of porphyrins and related macrocycles, part 43. Isolation and characterization of intermediates of coenzyme B12 biosynthesis, a cobyrinic acid triamide, the a,c-diamide and their Co-(5′-deoxy-5′-adenosyl) derivatives, from Propionibacterium shermanii
Chemistry & Biology
(1995)
2
527
(doi: 10.1016/1074-5521(95)90186-8)
Synthesis of bridged thiazolium salts as models for thiamin
Journal of the Chemical Society Perkin Transactions 1
(1995)
861
(doi: 10.1039/p19950000861)
Biosynthesis of vitamin B12: use of specific 13C-labelling for structural studies on factor IV
Chemical Communications
(1994)
193
(doi: 10.1039/c39940000193)
Biosynthesis of vitamin B12: Mechanistic studies on the transfer of a methyl group from C-11 to C-12 and incorporation of 18O
Journal of the Chemical Society, Chemical Communications
(1994)
2507
(doi: 10.1039/C39940002507)
Biosynthesis of vitamin B 12 : studies of the oxidative and lactone-forming steps by 18 O-labelling
Journal of the Chemical Society, Chemical Communications
(1994)
1649
(doi: 10.1039/c39940001649)
Design and synthesis of transition-state analogues for a cationic cyclisation
Journal of the Chemical Society, Perkin Transactions 1
(1994)
1997
(doi: 10.1039/p19940001997)
Synthesis of β-1-homonojirimycin and β-1-homomannojirimycin using the enzyme aldolase
J CHEM SOC PERK T 1
(1994)
231
(doi: 10.1039/p19940000231)
Biosynthesis of the indolizidine alkaloid cyclizidine: Incorporation of singly and doubly labelled precursors
Canadian Journal of Chemistry
(1994)
72
131
(doi: 10.1139/v94-021)
Biosynthesis of porphyrins and related macrocycles. Part 42. Pulse labelling experiments concerning the timing of cobalt insertion during vitamin B 12 biosynthesis
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(1994)
487
(doi: 10.1039/p19940000487)
Biosynthesis of porphyrins and related macrocycles. Part 41. Fate of oxygen atoms as precorrin-2 carrying eight labelled carboxyl groups ( 13C18O2H) is enzymatically converted into cobyrinic acid
Journal of the Chemical Society Perkin Transactions 1
(1993)
2893
Proof that the biosynthesis of vitamin B12 involves a reduction step in an anaerobic as well as an aerobic organism
Journal of the Chemical Society Chemical Communications
(1993)
515
(doi: 10.1039/c39930000515)
Biosynthesis of porphyrins and related macrocycles. Part 40. Synthesis of a spiro-lactam related to the proposed spiro-intermediate for porphyrin biosynthesis: Inhibition of cosynthetase
Journal of the Chemical Society Perkin Transactions 1
(1993)
2875
A novel stereoselective synthesis of the macrocycle of haem d1 that establishes its absolute configuration as 2R,7R
Journal of the Chemical Society, Chemical Communications
(1993)
275
(doi: 10.1039/c39930000275)
PREPARATION OF [4R-H-3]NADH, [4R-H-3]NADPH AND THE CORRESPONDING 4S-ISOMERS ALL WITH SUBSTANTIAL SPECIFIC ACTIVITIES
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
(1993)
1213
(doi: 10.1039/p19930001213)
BIOSYNTHESIS OF PORPHYRINS AND RELATED MACROCYCLES .40. SYNTHESIS OF A SPIRO-LACTAM RELATED TO THE PROPOSED SPIRO-INTERMEDIATE FOR PORPHYRIN BIOSYNTHESIS - INHIBITION OF COSYNTHETASE
J CHEM SOC PERK T 1
(1993)
2875
(doi: 10.1039/p19930002875)
Biosynthesis of porphyrins and related macrocycles. Part 41. Fate of oxygen atoms as precorrin-2 carrying eight labelled carboxyl groups ( 13 C 18 O 2 H) is enzymatically converted into cobyrinic acid
Journal of the Chemical Society Perkin Transactions 1
(1993)
2893
(doi: 10.1039/p19930002893)