137664-80-3

Upstream product

• 137765-35-6 (4R,5S,6R)-4-(2-Benzyloxy-ethyl)-6-iodomethyl-5-methyl-[1,3]dioxan-2-one 
• 254893-83-9 (S)-4-(1-{2-[(2S,3S,4R)-6-Benzyloxy-2,4-bis-(tert-butyl-dimethyl-silanyloxy)-3-methyl-hexyl]-[1,3]dithian-2-yl}-1-methyl-ethyl)-2-(4-methoxy-phenyl)-[1,3]dioxolane 
• 254893-81-7 (2S,3R,4R)-6-Benzyloxy-4-(tert-butyl-dimethyl-silanyloxy)-1-(2-{1-[(S)-2-(4-methoxy-phenyl)-[1,3]dioxolan-4-yl]-1-methyl-ethyl}-[1,3]dithian-2-yl)-3-methyl-hexan-2-ol 
• 254893-78-2 (S)-4-(1-[1,3]Dithian-2-yl-1-methyl-ethyl)-2-(4-methoxy-phenyl)-[1,3]dioxolane 
• 137664-69-8 [(1R,2R)-1-(2-Benzyloxy-ethyl)-2-(R)-oxiranyl-propoxy]-tert-butyl-dimethyl-silane 
• 137664-74-5 (3R,4S)-1-Benzyloxy-4-(R)-oxiranyl-pentan-3-ol 
• 137664-75-6 2-((S)-2,2-Diethyl-[1,3]dioxolan-4-yl)-2-methyl-propionaldehyde 
• 137664-76-7 (S)-3-[1,3]Dithian-2-yl-3-methyl-butane-1,2-diol 
• 137664-71-2 2-((S)-2,2-Diethyl-[1,3]dioxolan-4-yl)-2-methyl-propan-1-ol 
• 137664-79-0 (S)-3-{2-[(2S,3S,4R)-6-Benzyloxy-2,4-bis-(tert-butyl-dimethyl-silanyloxy)-3-methyl-hexyl]-[1,3]dithian-2-yl}-2-(4-methoxy-benzyloxy)-3-methyl-butan-1-ol 

Downstream Products

• 137765-34-5 (R)-Methoxy-phenyl-acetic acid (1S,2S)-3-{2-[(2S,3S,4R)-6-benzyloxy-2,4-bis-(tert-butyl-dimethyl-silanyloxy)-3-methyl-hexyl]-[1,3]dithian-2-yl}-2-(4-methoxy-benzyloxy)-3-methyl-1-vinyl-butyl ester 
• 137664-81-4 (S)-Methoxy-phenyl-acetic acid (1S,2S)-3-{2-[(2S,3S,4R)-6-benzyloxy-2,4-bis-(tert-butyl-dimethyl-silanyloxy)-3-methyl-hexyl]-[1,3]dithian-2-yl}-2-(4-methoxy-benzyloxy)-3-methyl-1-vinyl-butyl ester 
• 137664-67-6 (2S,3S,5S,7R,8R,9S)-7-(2-Benzyloxy-ethyl)-4,4,8-trimethyl-2-vinyl-1,6-dioxa-spiro[4.5]decane-3,9-diol 
• 162879-42-7 (2S,3S,5S,7R,8R,9S)-7-(2-Benzyloxy-ethyl)-3-(4-methoxy-benzyloxy)-4,4,8-trimethyl-2-vinyl-1,6-dioxa-spiro[4.5]decan-9-ol 
• 162991-28-8 (2R,3S,5S,7R,8R,9S)-7-(2-Benzyloxy-ethyl)-3-(4-methoxy-benzyloxy)-4,4,8-trimethyl-2-(R)-oxiranyl-1,6-dioxa-spiro[4.5]decan-9-ol 
• 218785-05-8 [(2R,3S,5S,7R,8S,9S)-7-(2-Benzyloxy-ethyl)-3-(4-methoxy-benzyloxy)-4,4,8-trimethyl-2-(R)-oxiranyl-1,6-dioxa-spiro[4.5]dec-9-yloxy]-tert-butyl-dimethyl-silane 
• 218785-35-4 (2S,3S,4R,5R,7R)-7-[(2S,3S,5S,7R,8S,9S)-7-(2-Benzyloxy-ethyl)-9-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-4,4,8-trimethyl-1,6-dioxa-spiro[4.5]dec-2-yl]-7-methoxy-2,4-dimethyl-heptane-1,3,5-triol 
• 218785-08-1 (1R,4R)-1-[(2S,3S,5S,7R,8S,9S)-7-(2-Benzyloxy-ethyl)-9-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-4,4,8-trimethyl-1,6-dioxa-spiro[4.5]dec-2-yl]-3-methylene-4-((4R,5S)-2,2,5-trimethyl-[1,3]dioxan-4-yl)-pentan-1-ol 
• 218785-31-0 {(2S,3S,5S,7R,8S,9S)-7-(2-Benzyloxy-ethyl)-3-(4-methoxy-benzyloxy)-2-[(1R,4R)-1-methoxy-3-methylene-4-((4R,5S)-2,2,5-trimethyl-[1,3]dioxan-4-yl)-pentyl]-4,4,8-trimethyl-1,6-dioxa-spiro[4.5]dec-9-yloxy}-tert-butyl-dimethyl-silane 
• 218785-37-6 C₆₁H₁₀₈O₁₁Si₃ 
• 218785-18-3 C₆₃H₁₂₅O₁₃PSi₅ 
• 218785-10-5 (1R,3R,4R)-1-[(2S,3S,5S,7R,8S,9S)-7-(2-Benzyloxy-ethyl)-9-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-4,4,8-trimethyl-1,6-dioxa-spiro[4.5]dec-2-yl]-1-methoxy-4-((4S,5S)-2,2,5-trimethyl-[1,3]dioxan-4-yl)-pentan-3-ol 
• 254893-88-4 (2S,3S,4R)-6-Benzyloxy-1-{2-[(2S,3S)-3-hydroxy-2-(4-methoxy-benzyloxy)-1,1-dimethyl-pent-4-enyl]-[1,3]dithian-2-yl}-3-methyl-hexane-2,4-diol 
• 254894-22-9 (2R,3S,5S,7R,8R,9S)-7-(2-Benzyloxy-ethyl)-3,9-bis-(4-methoxy-benzyloxy)-4,4,8-trimethyl-2-(R)-oxiranyl-1,6-dioxa-spiro[4.5]decane 

Relevant academic research and scientific papers

Total synthesis of (+)-calyculin A and (-)-calyculin B: Asymmetric synthesis of the C(9-25) spiroketal dipropionate subunit

An asymmetric synthesis of the stereochemically fully endowed C(9-25) spiroketal fragment (+)-BC of the calyculins (1-8) is described. Highlights of the synthesis include: a highly diastereoselective IBr-induced iodocarbonate cyclization to introduce the

CALYCULIN SYNTHETIC STUDIES. STEREOSELECTIVE CONSTRUCTION OF THE C(14)-C(25) SPIROKETAL SUBUNIT

A convergent, stereocontrolled synthesis of the spiroketal fragment of calyculins A-H has been achieved.Key transformations include the novel iodine monobromide-induced iodocarbonate cyclization of (+)-19, efficient coupling of epoxide (+)-14 with the ste