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5
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0347802444
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Recent Advances in Stereochemical Control: Multiple Asymmetric Induction
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Reviews on steroselection in aldol reaction
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(1984)
HETEROCYCLES
, vol.21
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Masamune1
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7
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0022047606
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Tin(II) compounds as synthetic control elements in organic synthesis
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Reviews on steroselection in aldol reaction
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(1986)
Pure and Applied Chemistry
, vol.58
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Mukaiyama1
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28
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-
85066115648
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O-Silylated Enolates - Versatile Intermediates for Organic Synthesis
-
Reviews on synthetic utility of enol silyl ethers
-
(1977)
Synthesis
, pp. 91
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-
Rasmussen1
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30
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-
0001704370
-
-
Reviews on synthetic utility of enol silyl ethers
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(1980)
Chimia
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Fleming1
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31
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0002211380
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Tilden Lecture. Some uses of silicon compounds in organic synthesis
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Reviews on synthetic utility of enol silyl ethers
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(1981)
Chemical Society Reviews
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-
Fleming1
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36
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84918139044
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-
6a,8 is modified as this.
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-
-
-
37
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33845554049
-
The reactions of trimethylchlorosilane with various nucleophiles in the gas phase using the flowing afterglow technique
-
For importance of pentacoordinate silicon species as reactive Intermediates, see
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(1982)
Organometallics
, vol.1
, pp. 1553
-
-
Damrauer1
DePuy2
Bierbaum3
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47
-
-
84918139043
-
-
2, -78 °C, 0.5 h) gave trimethylsilyl ethers of 34d (82%, erythro:threo = 73:27) and 34e (86%, erythro:threo = 69:31), respectively.
-
-
-
-
48
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0000169587
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-
Reaction of carbonyl compounds with powerful nucleophiles proceeds through such hypervalent silicon Intermediates. See
-
(1980)
Tetrahedron Lett.
, vol.21
, pp. 1357
-
-
Tsunoda1
Suzuki2
Noyorl3
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49
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-
0002198472
-
A facile synthesis of 2,3,4,6-tetra-O-benzyl-D-glucopyranosylidene acetals using trimethylsilyl trifluoromethanesulfonate catalyst.
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Reaction of carbonyl compounds with powerful nucleophiles proceeds through such hypervalent silicon Intermediates. See
-
(1981)
Chemistry Letters
, pp. 375
-
-
Yoshimura1
Horito2
Hashimoto3
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50
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0000223576
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-
Reaction of carbonyl compounds with powerful nucleophiles proceeds through such hypervalent silicon Intermediates. See
-
(1982)
J. Org. Chem.
, vol.47
, pp. 902
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-
Suzuki1
Takada2
Noyori3
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51
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84918139042
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-
Some decrease in selectivity in reaction of 41 and 5c by the use of TMSOTf/amine is perhaps due to higher temperature
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-
-
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57
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84918139041
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2, 25 °C).
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-
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64
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0011381262
-
Models for glycoside hydrolysis. Synthesis and hydrolytic studies of the anomers of a conformationally rigid acetal
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(1980)
The Journal of Organic Chemistry
, vol.45
, pp. 4641
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Van1
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76
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84918139039
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2a
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