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Back, Thomas G., Brunner, Kurt, Vijaya Krishna, M., Lai, Enoch K. Y. (1989) A selenosulfonation-based approach to (22S,23E)-6β-methoxy-3α,5-cyclo-5α-ergost-23-en-22-ol, a key intermediate for brassinolide synthesis. Canadian Journal of Chemistry, 67 (6). 1032-1037 doi:10.1139/v89-157

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Reference TypeJournal (article/letter/editorial)
TitleA selenosulfonation-based approach to (22S,23E)-6β-methoxy-3α,5-cyclo-5α-ergost-23-en-22-ol, a key intermediate for brassinolide synthesis
JournalCanadian Journal of Chemistry
AuthorsBack, Thomas G.Author
Brunner, KurtAuthor
Vijaya Krishna, M.Author
Lai, Enoch K. Y.Author
Year1989 (June 1)Volume67
Issue6
PublisherCanadian Science Publishing
DOIdoi:10.1139/v89-157Search in ResearchGate
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Mindat Ref. ID8316615Long-form Identifiermindat:1:5:8316615:4
GUID0
Full ReferenceBack, Thomas G., Brunner, Kurt, Vijaya Krishna, M., Lai, Enoch K. Y. (1989) A selenosulfonation-based approach to (22S,23E)-6β-methoxy-3α,5-cyclo-5α-ergost-23-en-22-ol, a key intermediate for brassinolide synthesis. Canadian Journal of Chemistry, 67 (6). 1032-1037 doi:10.1139/v89-157
Plain TextBack, Thomas G., Brunner, Kurt, Vijaya Krishna, M., Lai, Enoch K. Y. (1989) A selenosulfonation-based approach to (22S,23E)-6β-methoxy-3α,5-cyclo-5α-ergost-23-en-22-ol, a key intermediate for brassinolide synthesis. Canadian Journal of Chemistry, 67 (6). 1032-1037 doi:10.1139/v89-157
In(1989, June) Canadian Journal of Chemistry Vol. 67 (6) Canadian Science Publishing

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ANASTASIA, M., ALLEVI, P., CIUFFREDA, P., FIECCHI, A., SCALA, A. (1985) ChemInform Abstract: DIRECT TRANSFORMATION OF ERGOSTEROL TO (22S,23E)-6β-METHOXY-3α,5-CYCLO-5α-ERGOST-23-EN-22-OL, A KEY INTERMEDIATE FOR THE SYNTHESIS OF BRASSINOLIDE. Chemischer Informationsdienst, 16 (18) doi:10.1002/chin.198518304
Takatsuto, Suguru (1988) Synthesis of Dolicholide from (22E, 24R)-3α,5-Cyclo-5α-ergost-22-en-6-one. Agricultural and Biological Chemistry, 52. 2361-2363 doi:10.1080/00021369.1988.10869042
Back, Thomas G., Blazecka, Peter G., Krishna, M. Vijaya (1993) A new synthesis of castasterone and brassinolide from stigmasterol. A concise and stereoselective elaboration of the side chain from a C-22 aldehyde. Canadian Journal of Chemistry, 71 (2). 156-163 doi:10.1139/v93-022
Aburatani, Masakazu, Takeuchi, Tadashi, Mori, Kenji (1986) Efficient Synthesis of (22R,23R,24S)-22,23-Isopropylidenedioxy-5α-ergost-2-en-6-one, a Key Intermediate in the Preparation of Brassinolide. Agricultural and Biological Chemistry, 50. 3043-3047 doi:10.1080/00021369.1986.10867868
Brown, Frederick J., Massey, Ian J., Djerassi, Carl (1980) The mass spectrometric behavior of 3α,5-cyclo-5α-cholestan-6β-yl alkyl ethers. Canadian Journal of Chemistry, 58 (23). 2592-2599 doi:10.1139/v80-414
Darvesh, Sultan, Grant, Andrew S., Magee, David I., Valenta, Zdenek (1989) An approach to the synthesis of bruceantin. The synthesis of a tetracyclic intermediate. Canadian Journal of Chemistry, 67 (12). 2237-2240 doi:10.1139/v89-348
ABURATANI, Masakazu, TAKEUCHI, Tadashi, MORI, Kenji (1986) Efficient synthesis of (22R,23R,24S)-22,23-isopropylidenedioxy-5.ALPHA.-ergost-2-en-6-one, a key intermediate in the preparation of brassinolide. Agricultural and Biological Chemistry, 50. 3043-3047 doi:10.1271/bbb1961.50.3043
Ketuly, K. A., Yufit, D. S., Brooks, C. J. W., Freer, A. A. (1997) (20S)-6β-Methoxy-20-(p-toluenesulfonyloxymethyl)-3α,5-cyclo-5α-pregnane. Acta Crystallographica Section C Crystal Structure Communications, 53 (7) 981-982 doi:10.1107/s0108270197003570
Ishige, Masayoshi, Shiota, Michio (1975) Investigation on the Favorable Formation of 5α-Cholestan-3α-ol and 5-Cholesten-3α-ol by Catalytic Hydrogenation. Canadian Journal of Chemistry, 53 (12). 1700-1707 doi:10.1139/v75-241
Iriye, Ryozo, Sasakura, Masayuki (1977) Transformation of 6β-Bromo-4,4-dimethyl-1α,2α-epoxy-3α,5α-oxidocholestane into 6β-Bromo-4,4-dimethy1-3α,5α-oxido-5(10→1βH)abeo-10(19)-cholesten-2α-ol. Agricultural and Biological Chemistry, 41. 2109-2110 doi:10.1080/00021369.1977.10862822
Giroux, L., Back, M. H., Back, R. A. (1989) The photolysis of ethylene at 193 nm. Canadian Journal of Chemistry, 67 (7). 1166-1173 doi:10.1139/v89-176
 
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