(-)-cis-4-tert-butyldimethylsilyloxy-2-cyclopentenol

CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2635
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2636
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2637
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2638
title compound
Ausbeute 69.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2639
title compound
Ausbeute 64.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2640
title compound
Ausbeute 64.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)OC1C=CC(O[Si](C)(C)C(C)(C)C)C1
Reaction #2645
(-)-acetic acid 4-tert-butyldimethylsilyloxy-cyclopent-2-enyl ester
Ausbeute 51.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2647
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)O[C@@H]1C=C[C@H](O[Si](C)(C)C(C)(C)C)C1
Reaction #2653
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)O[C@@H]1CC[C@H](O)C1
Reaction #2657
title compound
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)O[C@@H]1CC[C@H](O)C1
Reaction #2661
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)O[C@H]1C=CC(=O)C1
Reaction #340698
above titled compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(C)(C)[Si](C)(C)O[C@H]1CC[C@@H](O)C1
Reaction #489714
title compound ( 32 )
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CC(C)(C)[Si](C)(C)O[C@H]1C=CC(=O)C1
Reaction #1054971
above titled compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_10
CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #1330389
(+)-(1S,4R)-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
CC(C)(C)[Si](C)(C)O[C@H]1CC[C@@H](O)C1
Reaction #1330390
(+)-(1R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-cyclopentanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
CC(C)(C)[Si](C)(C)O[C@H]1C=CC(=O)C1
Reaction #1949667
above titled compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_03
CC(C)(C)[Si](C)(C)O[C@H]1C=CC(=O)C1
Reaction #1972054
above titled compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_07
CC(C)(C)[Si](C)(C)O[C@H]1C=CC(=O)C1
Reaction #2275146
above titled compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_06
CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2481063
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_09
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