Search Results - "Jass, Paul A."
-
1
Use of N-trifluoroacetyl-protected amino acid chlorides in peptide coupling reactions with virtually complete preservation of stereochemistry
Published in Tetrahedron (03-11-2003)“…The use of protected amino acid chlorides for peptide coupling reactions has long been avoided due to the extensive racemization that commonly occurs during…”
Get full text
Journal Article -
2
Total synthesis of (+)-breynolide
Published in Journal of the American Chemical Society (01-05-1990)Get full text
Journal Article -
3
1,3-Dipolar cycloaddition annulations to the thieno[2,3-d]pyridazine, thieno[3,2-c]pyridine, and thieno[2,3-d]pyrimidine ring systems
Published in Journal of organic chemistry (01-02-1989)Get full text
Journal Article -
4
Regio- and stereoselective ring opening of epoxide with cyanoguanidine dianions, a facile synthesis of the KATP opener BMS-180448
Published in Tetrahedron: asymmetry (01-04-1998)Get full text
Journal Article -
5
Process Development of 5-Fluoro-3-[3-[4-(5-methoxy-4-pyrimidinyl)-1- piperazinyl]propyl]-1H-indole Dihydrochloride
Published in Organic process research & development (15-07-1997)“…5-Fluoro-3-[3-[4-(5-methoxy-4-pyrimidinyl)-1-piperazinyl]propyl]-1H-indole dihydrochloride (1) facilitates 5-HT neurotransmission and was an antidepressant…”
Get full text
Journal Article -
6
Regio- and stereoselective ring opening of epoxide with cyanoguanidine dianions, a facile synthesis of the K ATP opener BMS-180448
Published in Tetrahedron: asymmetry (24-04-1998)“…BMS-180448, (3S,4R)- 2, was prepared in 63% yield via a facile method which involved a new regio- and stereoselective ring opening of epoxide (3S,4S)- 12 with…”
Get full text
Journal Article -
7
Process Development of 5-Fluoro-3-[3-[4-(5-methoxy-4-pyrimidinyl)-1- piperazinyl]propyl]-1 H -indole Dihydrochloride
Published in Organic process research & development (01-07-1997)Get full text
Journal Article