140181-53-9

Upstream product

• 140181-52-8 (3aα,4α,5α,5aβ,6α,9aα,9bα)-(+/-)-decahydro-5-<3-<5-methyl-5-<<(1,1-dimethylethyl)dimethylsilyl>ethoxy>>-4,5-dihydroisoxazolyl>-4,5-dihydroxy-6-<4-methoxybenzyloxy>-2,2,4-5a,9,9-hexamethylnaphtho<1,2-d>-1,3-dioxol 
• 824-94-2 p-methoxybenzyl chloride 
• 140181-44-8 (1α,4β,4aα,8α,8aβ)-(+/-)-decahydro-1-formyloxime-8-methoxymethyloxy-2,5,5,8a-tetramethyl-1,2,3,4-naphthalenetetraol 
• 140181-50-6 (1α,2β,3β,4β,4aα,8α,8aβ)-(+/-)-2,3-epoxydecahydro-4-acetyloxy-1-<3-<5-methyl-5-<<(1,1-dimethylethyl)dimethylsilyl>ethoxy>>-4,5-dihydroisoxazolyl>-8-(4-methoxybenzyloxy)-2,5,5,8a-tetramethyl-1-naphthalenol 
• 140181-51-7 (1α,2β,3β,4β,4aα,8α,8aβ)-(+/-)-decahydro-1-<3-<5-methyl-5-<<(1,1-dimethylethyl)dimethylsilyl>ethoxy>>-4,5-dihydroisoxazolyl>-8-(4-methoxybenzyloxy)-2,5,5,8a-tetramethyl-1,2,3,4-naphthalenetetraol 
• 140181-47-1 (1α,2β,3β,4β,4aα,8α,8aβ)-(+/-)-2,3-epoxydecahydro-4-acetyloxy-1-formyl-(O-acetyloxime)-2,5,5,8a-tetramethyl-1,8-naphthalenediol 
• 140181-35-7 (1α,4aβ,8α,8aβ)-(+/-)-1,2,3,4,8,8a-hexahydro-8-ethoxyethynyl-1-methoxymethyloxy-(4aH)-5-oxo-4,4,7,8a-tetramethylnaphthalen-8-ol 
• 140181-43-7 (4β,4aβ,5α,8aα)-(+/-)-4a,5,6,7,8,8a-hexahydro-4-formyloxime-4-hydroxy-5-methoxymethyloxy-3,4a,8,8-tetramethyl-1(4H)-naphthalenone 
• 140181-34-6 (1α,4aβ,8aβ)-(+/-)-1,2,3,4-tetrahydro-1-methoxymethyloxy-4,4,7,8a-tetramethyl-(4aH,8aH)-naphthalene-5,8-dione 
• 124666-38-2 (2β,4α,4aβ,8α,8aβ)-(+/-)-octahydro-4-acetyloxy-8-hydroxy-2,5,5,8a-tetramethyl-(2H)-naphthalen-1-one 
• 140181-33-5 (6aβ,9aβ,9bβ)-(+/-)-6a,7,8,9,9a,9b-hexahydro-4,7,7,9b-tetramethyl-(5H)-naphtho<1.8-de>-1,3-dioxin-6-one 
• 140181-32-4 (6α,6aβ,9aβ,9bβ)-(+/-)-6-hydroxy-5,6,6a,7,8,9,9a,9b-octahydro-4,7,7,9b-tetramethyl-naphtho<1.8-de>-1,3-dioxin 
• 123218-01-9 (1α,4aβ,8aβ)-(+/-)-1,2,3,4-tetrahydro-1-hydroxy-4,4,7,8a-tetramethyl-(4aH,8aH)-naphthalene-5,8-dione 
• 140181-36-8 (4S,4aS,5R,8aS)-4-((Z)-2-Ethoxy-vinyl)-4-hydroxy-5-methoxymethoxy-3,4a,8,8-tetramethyl-4a,5,6,7,8,8a-hexahydro-4H-naphthalen-1-one 

Relevant academic research and scientific papers

A formal total synthesis of (±)-forskolin through [3 + 2] nitrile oxide cycloaddition chemistry

A formal synthesis of (±)-forskolin 1 has been accomplished utilizing 1,3-dipolar nitrile oxide cycloaddition chemistry either for an alternative and convenient preparation of the key enedione starting building block 3 as well as for the introduction of t