In F. Dean Toste's 2007 total synthesis of (+)-Fawcettimine (Angew Chem, 46 (40), 7671-7673), a Robinson Annulation was a critical first step in the reaction of ketoester (1) with crotonaldehyde (2) to provide 3 on a multi-gram scale in high yield with an important stereocenter set (R) in high ee (88%) by the use of a proline-derived chiral catalyst. Not worrying about the stereocenters, a detailed, step-wise, arrow pushing mechanisms for the Robinson Annulation to provide 3 is shown. Select the best answer that fills

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Chapter1: Chemical Foundations
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In F. Dean Toste's 2007 total synthesis of (+)-Fawcettimine (Angew Chem, 46
(40), 7671-7673), a Robinson Annulation was a critical first step in the
reaction of ketoester (1) with crotonaldehyde (2) to provide 3 on a multi-gram
scale in high yield with an important stereocenter set (R) in high ee (88%) by
the use of a proline-derived chiral catalyst. Not worrying about the
stereocenters, a detailed, step-wise, arrow pushing mechanisms for the
Robinson Annulation to provide 3 is shown. Select the best answer that fills
in both missing components correctly in the boxes shown for 1.) and 2.).
The R group is an allyl group in all answers.
10% Proline-derived
chiral catalyst
O'Bu
NaOH (aq), 0°C, 60h
O'Bu
1
2
3
Mechanism
1.)
O'Bu
O'Bu
O'Bu
O'Bu
e:ö:
:0:
R.
: OH
1
H.
R= Ally
OH
2)
R.
O'Bu
R.
O'Bu
O'Bu
:0:
но
Transcribed Image Text:In F. Dean Toste's 2007 total synthesis of (+)-Fawcettimine (Angew Chem, 46 (40), 7671-7673), a Robinson Annulation was a critical first step in the reaction of ketoester (1) with crotonaldehyde (2) to provide 3 on a multi-gram scale in high yield with an important stereocenter set (R) in high ee (88%) by the use of a proline-derived chiral catalyst. Not worrying about the stereocenters, a detailed, step-wise, arrow pushing mechanisms for the Robinson Annulation to provide 3 is shown. Select the best answer that fills in both missing components correctly in the boxes shown for 1.) and 2.). The R group is an allyl group in all answers. 10% Proline-derived chiral catalyst O'Bu NaOH (aq), 0°C, 60h O'Bu 1 2 3 Mechanism 1.) O'Bu O'Bu O'Bu O'Bu e:ö: :0: R. : OH 1 H. R= Ally OH 2) R. O'Bu R. O'Bu O'Bu :0: но
c.) 1.)
b.) 1) 1
a) 1.)
2)
2)
2)
:0:
:0:
::
R.
O'Bu
R
O'Bu
O'Bul
****!
HO
HO
но
f.) 1.)
1
e) 1.)
1.
d) 1.)
2)
2)
:0:
2)
:0:
:0:
R
R.
O'Bu
O'Bu
R.
O'Bu
**
HO
HO
a.)
O b.)
:
Transcribed Image Text:c.) 1.) b.) 1) 1 a) 1.) 2) 2) 2) :0: :0: :: R. O'Bu R O'Bu O'Bul ****! HO HO но f.) 1.) 1 e) 1.) 1. d) 1.) 2) 2) :0: 2) :0: :0: R R. O'Bu O'Bu R. O'Bu ** HO HO a.) O b.) :
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