Diastereoselection in 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate

Takahashi, M. ; Suzuki, H. ; Moro-oka, Y. ; Ikawa, T.

Amsterdam : Elsevier
ISSN:
0040-4039
Source:
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
Topics:
Chemistry and Pharmacology
Type of Medium:
Electronic Resource
URL:
_version_ 1798291365537251328
autor Takahashi, M.
Suzuki, H.
Moro-oka, Y.
Ikawa, T.
autorsonst Takahashi, M.
Suzuki, H.
Moro-oka, Y.
Ikawa, T.
book_url http://linkinghub.elsevier.com/retrieve/pii/S0040-4039(00)88688-8
datenlieferant nat_lic_papers
fussnote Remarkable diastereoselection, with (E)-alkenyl alkyl acetal giving selectively the erythro α-alkyl-β-alkoxyaldehyde, and (Z)-acetal leading preferentially to the threo isomer, is observed in the 1,3-O- to - C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate.
hauptsatz hsatz_simple
identnr NLZ176122737
issn 0040-4039
journal_name Tetrahedron Letters
materialart 1
package_name Elsevier
publikationsort Amsterdam
publisher Elsevier
reference 23 (1982), S. 4031-4034
search_space articles
shingle_author_1 Takahashi, M.
Suzuki, H.
Moro-oka, Y.
Ikawa, T.
shingle_author_2 Takahashi, M.
Suzuki, H.
Moro-oka, Y.
Ikawa, T.
shingle_author_3 Takahashi, M.
Suzuki, H.
Moro-oka, Y.
Ikawa, T.
shingle_author_4 Takahashi, M.
Suzuki, H.
Moro-oka, Y.
Ikawa, T.
shingle_catch_all_1 Takahashi, M.
Suzuki, H.
Moro-oka, Y.
Ikawa, T.
Diastereoselection in 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate
0040-4039
00404039
Elsevier
shingle_catch_all_2 Takahashi, M.
Suzuki, H.
Moro-oka, Y.
Ikawa, T.
Diastereoselection in 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate
0040-4039
00404039
Elsevier
shingle_catch_all_3 Takahashi, M.
Suzuki, H.
Moro-oka, Y.
Ikawa, T.
Diastereoselection in 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate
0040-4039
00404039
Elsevier
shingle_catch_all_4 Takahashi, M.
Suzuki, H.
Moro-oka, Y.
Ikawa, T.
Diastereoselection in 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate
0040-4039
00404039
Elsevier
shingle_title_1 Diastereoselection in 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate
shingle_title_2 Diastereoselection in 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate
shingle_title_3 Diastereoselection in 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate
shingle_title_4 Diastereoselection in 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate
sigel_instance_filter dkfz
geomar
wilbert
ipn
albert
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source_archive Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
timestamp 2024-05-06T08:31:28.716Z
titel Diastereoselection in 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate
titel_suche Diastereoselection in 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate
Remarkable diastereoselection, with (E)-alkenyl alkyl acetal giving selectively the erythro α-alkyl-β-alkoxyaldehyde, and (Z)-acetal leading preferentially to the threo isomer, is observed in the 1,3-O- to - C-alkyl migration reaction of 1-alkenyl alkyl acetals catalyzed by boron trifluoride etherate.
topic V
uid nat_lic_papers_NLZ176122737