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Stereoselective Reduction Using Sodium Triacetoxyborodeuteride: Synthesis of Methyl 2,3-Di-O-benzyl-α-d-(4-2H)-glucopyranoside

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Standard Standard

Stereoselective Reduction Using Sodium Triacetoxyborodeuteride: Synthesis of Methyl 2,3-Di-O-benzyl-α-d-(4-2H)-glucopyranoside. / Mobarak, H.; Engstrom, O.; Lahmann, Martina et al.
Carbohydrate Chemistry: Proven Synthetic Methods: Volume 3. 2015. ed. CRC Press, 2015. p. 81-88.

Research output: Chapter in Book/Report/Conference proceeding › Chapter

HarvardHarvard

Mobarak, H, Engstrom, O, Lahmann, M, Widmalm, G, Roy, R (ed.) & Vidal, S (ed.) 2015, Stereoselective Reduction Using Sodium Triacetoxyborodeuteride: Synthesis of Methyl 2,3-Di-O-benzyl-α-d-(4-2H)-glucopyranoside. in Carbohydrate Chemistry: Proven Synthetic Methods: Volume 3. 2015 edn, CRC Press, pp. 81-88.

APA

Mobarak, H., Engstrom, O., Lahmann, M., Widmalm, G., Roy, R. (Ed.), & Vidal, S. (Ed.) (2015). Stereoselective Reduction Using Sodium Triacetoxyborodeuteride: Synthesis of Methyl 2,3-Di-O-benzyl-α-d-(4-2H)-glucopyranoside. In Carbohydrate Chemistry: Proven Synthetic Methods: Volume 3 (2015 ed., pp. 81-88). CRC Press.

CBE

Mobarak H, Engstrom O, Lahmann M, Widmalm G, Roy R, Vidal S, ed. 2015. Stereoselective Reduction Using Sodium Triacetoxyborodeuteride: Synthesis of Methyl 2,3-Di-O-benzyl-α-d-(4-2H)-glucopyranoside. In Carbohydrate Chemistry: Proven Synthetic Methods: Volume 3. 2015 ed. CRC Press. pp. 81-88.

MLA

Mobarak, H. et al. "Stereoselective Reduction Using Sodium Triacetoxyborodeuteride: Synthesis of Methyl 2,3-Di-O-benzyl-α-d-(4-2H)-glucopyranoside". Carbohydrate Chemistry: Proven Synthetic Methods: Volume 3. 2015 udg., CRC Press. 2015, 81-88.

VancouverVancouver

Mobarak H, Engstrom O, Lahmann M, Widmalm G, Roy R, (ed.), Vidal S, (ed.). Stereoselective Reduction Using Sodium Triacetoxyborodeuteride: Synthesis of Methyl 2,3-Di-O-benzyl-α-d-(4-2H)-glucopyranoside. In Carbohydrate Chemistry: Proven Synthetic Methods: Volume 3. 2015 ed. CRC Press. 2015. p. 81-88

Author

Mobarak, H. ; Engstrom, O. ; Lahmann, Martina et al. / Stereoselective Reduction Using Sodium Triacetoxyborodeuteride: Synthesis of Methyl 2,3-Di-O-benzyl-α-d-(4-2H)-glucopyranoside. Carbohydrate Chemistry: Proven Synthetic Methods: Volume 3. 2015. ed. CRC Press, 2015. pp. 81-88

RIS

TY - CHAP

T1 - Stereoselective Reduction Using Sodium Triacetoxyborodeuteride: Synthesis of Methyl 2,3-Di-O-benzyl-α-d-(4-2H)-glucopyranoside

AU - Mobarak, H.

AU - Engstrom, O.

AU - Lahmann, Martina

AU - Widmalm, G.

A2 - Roy, R.

A2 - Vidal, S.

PY - 2015/5/27

Y1 - 2015/5/27

N2 - Volumes in the Proven Synthetic Methods Series address the concerns many chemists have regarding irreproducibility of synthetic protocols, lack of characterization data for new compounds, and inflated yields reported in chemical communications―trends that have recently become a serious problem. Featuring contributions from world-renowned experts and overseen by a highly respected series editor, Carbohydrate Chemistry: Proven Synthetic Methods, Volume 3 compiles reliable protocols for the preparation of intermediates for carbohydrate synthesis or other uses in the glycosciences. Exploring carbohydrate chemistry from both the academic and industrial points of view, this unique resource brings together useful information into one convenient reference. To ensure reproducibility, an independent checker has verified the experimental parts involved by repeating the protocols or using the methods. The book includes new or more detailed versions of previously published protocols as well as those published in not readily available journals. The essential characteristics of the protocols presented are reliability and the expectation of wide utility in the carbohydrate field. The protocols presented will be of wide use to a wide range of readers in the carbohydrate field, including undergraduates taking carbohydrate workshops.

AB - Volumes in the Proven Synthetic Methods Series address the concerns many chemists have regarding irreproducibility of synthetic protocols, lack of characterization data for new compounds, and inflated yields reported in chemical communications―trends that have recently become a serious problem. Featuring contributions from world-renowned experts and overseen by a highly respected series editor, Carbohydrate Chemistry: Proven Synthetic Methods, Volume 3 compiles reliable protocols for the preparation of intermediates for carbohydrate synthesis or other uses in the glycosciences. Exploring carbohydrate chemistry from both the academic and industrial points of view, this unique resource brings together useful information into one convenient reference. To ensure reproducibility, an independent checker has verified the experimental parts involved by repeating the protocols or using the methods. The book includes new or more detailed versions of previously published protocols as well as those published in not readily available journals. The essential characteristics of the protocols presented are reliability and the expectation of wide utility in the carbohydrate field. The protocols presented will be of wide use to a wide range of readers in the carbohydrate field, including undergraduates taking carbohydrate workshops.

M3 - Chapter

SN - 978-1466583573

SP - 81

EP - 88

BT - Carbohydrate Chemistry: Proven Synthetic Methods

PB - CRC Press

ER -