942618-52-2

Upstream product

• 942618-63-5 C₂₇H₃₇NO₆Si 
• 727411-42-9 (2E,4E,6E,12E)-(8R,10S,14R)-8,10,12,14-( tetramethyl)hexadeca-2,4,6,12-tetraenoic acid 
• 942618-32-8 (3S,5S,10S)-3-benzyloxycarbonylamino-10-triethylsilyloxy-1-oxaspiro[4,5]dec-6-ene-2,8-dione 
• 942618-33-9 (3S,5S,8R,10S)-3-benzyloxycarbonylamino-8-hydroxy-10-triethylsilyloxy-1-oxaspiro[4,5]dec-6-en-2-one 
• 942618-34-0 (3S,5S,6R,7R,8R,10S)-3-benzyloxycarbonylamino-6,7-epoxy-8-hydroxy-10-triethylsilyloxy-1-oxaspiro[4,5]dec-6-en-2-one 
• 942618-45-3 (3S,5S,8R,10S)-8-acetoxy-3-benzyloxycarbonylamino-10-triethylsilyloxy-1-oxaspiro[4,5]dec-6-en-2-one 
• 942618-46-4 (1S,2'S,4R,6S)-4-acetoxy-1-(2'-benzyloxycarbonylamino-3'-hydroxy-propyl)-6-triethylsilyloxy-2-cyclohexen-1-ol 
• 942618-47-5 (1S,2'S,4R,6S)-4-acetoxy-1-(2'-benzyloxycarbonylamino-3'-hydroxy-propyl)-6-hydroxy-2-cyclohexen-1-ol 
• 942618-48-6 (1S,2'S,4R,6S)-4-acetoxy-1-(2'-benzyloxycarbonylamino-3'-tert-butyldiphenylsilyloxy-propyl)-6-hydroxy-2-cyclohexen-1-ol 
• 942618-49-7 (1R,2S,2'S,3S,4R,6S)-4-acetoxy-1-(2'-benzyloxycarbonylamino-3'-tert-butyldiphenylsilyloxy-propyl)-2,3-epoxy-6-hydroxy-2-cyclohexen-1-ol 
• 942618-30-6 (4S)-4-benzyloxycarbonylamino-6',7'-epoxy-1',3,4,4',4'a,8'a-hexahydrospiro[furan-2(5H),5'(8'H)-1',4'-methanonaphthalene]-5',8'-dione 
• 942618-57-7 C₂₂H₂₃NO₆ 
• 942618-31-7 (1S,4R,4'S,4aS,5S,6S,8aR)-4'-benzyloxycarbonylamino-6-triethylsilyloxy-1,3',4',4,4a,6,7,8a-octahydrospiro[furan-2'(5H),5(8H)-1,4-methanonaphthalene]-5',8-dione 
• 92886-86-7 tert-butyldiphenylsilyl triflate 

Downstream Products

• 942618-53-3 (2'S,2''E,4S,4''E,5S,6S,6''E,8''R,10''S,12''E,14''R)-4,5-epoxy-6-hydroxy-6-[2'-(8'',10'',12'',14''-tetramethylhexadeca-2'',4'',6'',12''-tetraenoylamino)-3'-tert-butyldiphenylsilyloxy-propyl]-2-cyclohexen-1-one 

Relevant academic research and scientific papers

Stereoselective total synthesis of (+)-scyphostatin via a π-facially selective Diels-Alder reaction

(Chemical Equation Presented) A stereoselective total synthesis of scyphostatin is described. The hydrophilic moiety was stereoselectively synthesized via (i) a highly π-facially selective Diels-Alder reaction of a spirolactone generated from L-tyrosine a