Inventor

GRABOWSKI EDWARD J J

US34 patents

⚠️ This page may combine multiple inventors who share the name “GRABOWSKI EDWARD J J”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.

GRABOWSKI EDWARD J J

MERCK & CO INC

Dihydroxy open-acid and salts of HMG-CoA reductase inhibitors

Efficient synthesis of a 1,4-dihydro2H-3,1-benzoxazin-2-one

Asymmetric synthesis of (-)-6-chloro-4-cyclopropyl-ethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxanzin-2-one

Enantiospecific synthesis of s-(+)-5,6-dihydro-4-(r-amino)-4h-thieno(2,3-b)thiopyran-2-sulfonamide-7,7-dioxide

Crystalline salts of L or (S)-3-(3,4-dihydroxyphenyl)-2-methylalanine esters and process

Process for 2-(aminoalkylthio) carbapenems

Asymmetric synthesis of (-)6-chloro-4-cyclopropyl-ethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one

Converting an alcohol to an azide with SN 2 inversion using a phosphoryl azide

Asymmetric synthesis of (S)-(-)-6-chloro-4- cyclopropyl-3,4-dihydro-4-[(2-pyridyl)ethynyl]-2(1H)-quinazolinone

(S)-Alkyl 3-(thien-2-ylthio)butyrate and analogs and synthesis thereof

Resolution of a carboxylic acid

Process for resolution and racemization of amines with acidic α-hydrogens

Preparation of 2-Deutero-D-serine

Process for preparing indenyl acetic acids

Process for crystalline salts of L or (S)-3-(3,4-dihydroxyphenyl)-2-methylalanine esters

Efficient synthesis of A 1,4-dihydro-2H-3,1-benzoxazin-2-one

Process for enhancing the optical purity

Chiral resolution process

Trifluoromethylbenzyl containing quaternary salts

Process for racemizing an enantiomer of 5,6-dihydro-4-alkylamino-4H-thieno(or furo) [2,3-B]-thiopyran-2-sulfonamide-7,7-dioxide

Process for preparing a manipulated enantiomer mixture by asymmetric chiral phase transfer catalysis

Synthesis of racemic 3-fluoro-alanine and its salts

Synthesis of racemic 2-deutero-3-fluoro-alanine and its salts

4,9-Diazatricyclo[6.2.2.02,7 ]dodec-11-enes

Diazatetracyclododecanes

Boronic acid compound

Preparation of 2-aryl carbapenems

Synthesis of methylthiophenyl hydroxyketones

7-(Amidinothio)acetamido-7-methoxy cephalosporins

Process for preparing 5,11-diazatetracyclododecanes

Enzymic process for preparing leukotriene antagonists

Rearrangement process and tricyclic and tetracyclic compounds

Process to derivatives of piperizinylcamphorsulfonyl oxytocin antagonists

(unassigned)

Antibiotic synthesis